Haplogroup O-M175
Haplogroup O-M175 | |
---|---|
File:Haplogrupo O (ADN-Y).PNG | |
Possible time of origin | 41,750 (95% CI 30,597<-> 46,041) years ago[1] 44,700 or 38,300 ybp[2] |
Coalescence age | 33,943 (95% CI 25,124 <-> 37,631) years (Karmin 2022[1]) 35,000 or 30,000 years ago depending on mutation rate[2] |
Possible place of origin | Southeast Asia or East Asia |
Ancestor | NO |
Descendants | Primary: O1 (O-F265); O2 (O-M122) Secondary: O1a (O-M119); O1b (O-M268); O2a (O-M324); O2b (O-F742) |
Defining mutations | M175 (+ numerous other SNPs).[3] |
Haplogroup O, also known as O-M175, is a human Y-chromosome DNA haplogroup. It is primarily found among populations in Southeast Asia and East Asia. It also is found in various percentages of populations of the Russian Far East, South Asia, Central Asia, Caucasus, Crimea, Ukraine, Iran, Oceania, Madagascar and the Comoros. Haplogroup O is a primary descendant of haplogroup NO-M214. The O-M175 haplogroup is very common amongst males from East and Southeast Asia. It has two primary branches: O1 (O-F265) and O2 (O-M122). O1 is found at high frequencies amongst males native to Southeast Asia, Taiwan, the Japanese Archipelago, the Korean Peninsula, Madagascar and some populations in southern China and Austroasiatic speakers of India. O2 is found at high levels amongst Han Chinese, Tibeto-Burman populations (including many of those in Yunnan, Tibet, Burma, Northeast India, and Nepal), Manchu, Mongols (especially those who are citizens of the PRC), Koreans, Vietnamese, Filipinos, Japanese, Thais, Polynesians, Miao people, Hmong, the Naiman tribe of Kazakhs in Kazakhstan,[4] Kazakhs in the southeast of Altai Republic,[5] and Kazakhs in the Ili area of Xinjiang.[6]
Origins
Haplogroup O-M175 is a descendant haplogroup of Haplogroup NO-M214, and first appeared according to different theories either in Southeast Asia (see Rootsi 2006, TMC 1998, Shi 2005, and Bradshaw Foundation) or East Asia (see ISOGG 2012) approximately 40,000 years ago (or between 31,294 and 51,202 years ago according to Karmin et al. 2015).[7][8] Haplogroup O-M175 is one of NO-M214's two branches. The other is Haplogroup N, which is common throughout North Eurasia.
Distribution
This haplogroup appears in high to moderate frequencies in most populations in both East Asia and Southeast Asia, and it is almost exclusive to that region. It is almost nonexistent in Western Siberia, Western Asia, Europe, most of Africa, India and the Americas, where its presence may be the result of recent migrations. However, certain O subclades do achieve significant frequencies among some populations of Central Asia, South Asia, and Oceania. For example, one study found it at a rate of 67% among the Naimans, a tribe in Kazakhstan,[4] even though the rate among Kazakhs in general is only about 3.3% to 10.8%(Wells et al. 2001).[4][9] (It is notable that 75% of cases of haplogroup O-M175 observed in the Kazakh sample of Ashirbekov et al. 2017, of which 10.8% have been found to belong to haplogroup O-M175, have been contributed by the Naimans themselves; only 3.1% of the remainder of the Kazakh sample with the Naimans excluded belong to haplogroup O-M175.) It has been estimated that 25% of the entire male population of the world carries different subclades of O.[8][10] Karafet et al. (2015) have assigned the Y-DNA of 46.2% (12/26) of a sample of Papuan from Pantar Island to haplogroup NO-M214;[11] considering their location in the Malay Archipelago, all or most of these individuals should belong to haplogroup O-M175. An association with the spread of Austronesian languages in late antiquity is suggested by significant levels of O-M175 among island populations of the South Pacific and Indian Ocean, including the East African littoral. For example, Haplogroup O-M50 has even been found in Bantu-speaking populations of the Comoros along 6% of O-MSY2.2(xM50),[12] while both O-M50 and O-M95(xM88) occur commonly among the Malagasy people of Madagascar with a combined frequency of 34%.[13][14] O-M175 has been found in 28.1% of Solomon Islanders from Melanesia.[15] 12% of Uyghurs (Wells et al. 2001), 6.8% of Kalmyks[16] (17.1% of Khoshuud, 6.1% of Dörwöd, 3.3% of Torguud, 0% of Buzawa), 6.2% of Altaians (Kharkov et al. 2007), 4.1% of Uzbeks on average but Uzbeks from Bukhara 12.1%, Karakalpaks (Uzbekistan) 11.4%, Sinte (Uzbekistans) 6.7% (Wells et al. 2001) and 4.0% of Buryats.[17] In the Caucasus region it has been found in the Nogais 6%[18] but 5.3% in the Karan Nogais, it is also found in the Dargins of Dargwa speakers at 2.9%.[19] In the Iranic population, it is found in Iranian (Esfahan) at 6.3% (Wells et al. 2001), 8.9% of Tajiks in Afghanistan[20] 4.2% in the Pathans in Pakistan (Firasat 2007) but 1% in Afghanistan,[citation needed] 3.1% in Burusho (Firasat 2007). Haplogroup O-M175 ranges in various moderate to high frequencies in the ethnic minorities of South Africa. The frequency of this haplogroup is 6.14% in the Cape colored population,[21] 18% in Cape Coloured Muslim, 38% in Cape Indian Muslims and 10% in Cape Other Muslims.[21] It's found 11.5% in the Réunion Creole.[22] Haplogroup O-M175 had also been found in Latin America and Caribbean as a result of massive Chinese male migration from the 19th century. It was found in the Jamaicans at 3.8%,[23] and in Cubans, 1.5%.[24] Haplogroup O-M175 has been found in 88.7% of Asian American. 1.6% in Hispanic American, White Americans 0.5%, and 0.3% in African American.[25] Another study gives 0.5% African American.[26] Among the sub-branches of haplogroup O-M175 are O-M119(O1a), O-M268(O1b), and O-M122(O2). Y Haplogroup O3-M122 makes up the majority of Jadoon's males, the same haplogroup carried by the majority (50-60%) of Han Chinese. 82.5% of Jadoon men carrying Q-MEH2 and O3-M122 which are both of East Asian origin. O3-M122 was absent in the Sayyid (Syed) population and appeared in low numbers among Tanolis, Gujars and Yousafzais. There appears to be founder affect in the O3-M122 among the Jadoon.[27][28][29] 76.32% of Jadoon men carry O3-M122 while 0.75% of Tanolis, 0.81% of Gujars and 2.82% of Yousafzais carry O3-M122.[30][31] Russians in China East Asian haplogroup O made up 58% of their Y haplogroup. O3-M122 specifically made up 47% of the Russian sample.[32] The East Asian Y haplogroup O3-M122 was found in 47% of Russian males in China. In another test the East Asian paternal Y Haplogroup O made up 58% of Russian males samples in China.[33] Haplogroup O was found in 1%-1.2% of Persians in one sample.[34][35][36][better source needed][37][better source needed] O3-M122 is the commonly shared genetic signature of Sino-Tibetan speaking ethnicities.[38]
O-M175*
A broad survey of Y-chromosome variation among populations of central Eurasia found haplogroup O-M175(xM119,M95,M122) in 31% (14/45) of a sample of Koreans and in smaller percentages of Crimean Tatars (1/22 = 4.5%), Tajiks (1/16 = 6.25% Dushanbe, 1/40 = 2.5% Samarkand), Uyghurs (2/41 = 4.9%), Uzbeks (1/68 = 1.5% Surxondaryo, 1/70 = 1.4% Xorazm), and Kazakhs (1/54 = 1.9%) (Wells et al. 2001). However, nearly all of the purported Korean O-M175(xM119,M95,M122) Y-chromosomes may belong to Haplogroup O-M176,[Note 1] and later studies do not support the finding of O-M175* among similar population samples (Xue 2006, Kim 2011). The reported examples of O-M175(xM119,M95,M122) Y-chromosomes that have been found among these populations might therefore belong to Haplogroup O-M268*(xM95,M176) or Haplogroup O-M176 (O1b2). A study published in 2013 found O-M175(xM119, M95, M176, M122) Y-DNA in 5.5% (1/18) Iranians from Teheran, 5.4% (2/37) Tajiks from Badakhshan Province of Afghanistan, and 1/97 Mongols from northwest Mongolia, while finding O-M176 only in 1/20 Mongols from northeast Mongolia.[39]
O-F265 (O1)
O1a-M119 and O1b-M268 share a common ancestor, O1-F265 (a.k.a. O-F75) approximately 33,181 (95% CI 24,461 to 36,879) YBP.[1][40] O1-F265, in turn, coalesces to a common ancestor with O2-M122 approximately 33,943 (95% CI 25,124 to 37,631) YBP.[1] Thus, O1-F265 should have existed as a single haplogroup parallel to O2-M122 for a duration of approximately 762 years (or anywhere from 0 to 13,170 years considering the 95% CIs and assuming that the phylogeny is correct) before breaking up into its two extant descendant haplogroups, O1-MSY2.2 and O1b-M268.
O-M119 (O1a)
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O-M119 (which was known briefly as O-MSY2.2, until the SNP MSY2.2 was found to be unreliable) is found frequently in Austronesian-speaking people, with a moderate distribution in southern and eastern Chinese and Kra-dai peoples.
O-M268 (O1b)
- O-K18 Naxi[41]
- O-CTS4040
- O-MF56251 Observed sporadically in China (Guangxi,[41][42] Guangdong,[42] Sichuan,[42] Zhejiang,[42] Jiangsu,[42] Beijing[42]), Thailand (Phuan,[43] Yuan,[43] Central Thai[43]), Vietnam (Nùng,[43] Tày[43])
- O-Page59/CTS10887 Found among North Han Chinese (5%), East Han Chinese (4%), South Han Chinese (3%) [44]
- O-F4070
- O-MF106398 Observed sporadically in China (Guangdong, Henan, Hubei, Jiangxi, Sichuan, Zhejiang, Guangxi, Heilongjiang, Jiangsu, Shandong[42])
- O-F779/F993/F3135 China,[42] Vietnam (Lahu[45]), Qatar[46]
- O-MF107014 Observed sporadically in China (Jiangsu, Anhui, Heilongjiang[42])
- O-CTS5160/MF61620 China (Han,[41] mostly Guangdong or Fujian[42])
- O-F2064/F1759 China (Han from Fujian,[41] Shandong[41]), Singapore,[41] Vietnam (Sila,[45] Hanhi,[45] Kinh[45]), Korea[41]
- O-PH2797/CTS1127 China (especially Shandong, Jiangsu, Liaoning, Hebei, Anhui, Beijing, Henan, and Shanghai[42])
- O-Y148532 China (Shandong, Heilongjiang, Liaoning, Jilin, Jiangsu, Shanghai, Sichuan,[41] Beijing, Shaanxi[42]), Afghanistan (Hazara[41])
- O-Y239146/MF31164 Singapore,[41] Taiwan[41]
- O-Y47392/MF17288 China (Zhejiang[41])
- O-BY182144/Y157814 China (Shandong,[41][42] Gansu[42]), Taiwan[47]
- O-PH4822 China (Beijing,[41] Jiangsu[41])
- O-F417/M1654/CTS469 Japan (Tokyo[41])
- O-CTS9996/PF4341 Philippines[47]
- O-F4070
- O-PK4
- O-F838 Found in about 1.4% of Han Chinese[44] (and esp. in Hunan, Chongqing, Jiangxi, Sichuan, Guizhou[42])
- O-M95
- O-CTS350 China (Ningxia, Yunnan, Heilongjiang, Hunan, Shaanxi, Anhui, etc.[42])
- O-M1310
- O-Y172653/Y172877 Found in China (esp. Zhejiang, Fujian, Guangdong, Sichuan, Hunan, Jiangxi, Hubei, Chongqing[42]) and Japan[42]
- O-F1803/M1348 China (Zhejiang, Shandong, Beijing, Guangdong, Hubei, Sichuan, Jiangsu, Shanghai, etc.[42])
- O-ACT721/ACT1038 Found sporadically in China (Zhejiang,[42] Anhui,[42] Hunan,[42] Hainan,[41] Tianjin,[42] Beijing,[42] Liaoning,[41] Heilongjiang[42])
- O-F789/M1283 Found in China (Blang,[49] Palaung,[49] Wa,[49] Dai,[41][50] Yi,[41][50] Naxi), Vietnam, Cambodia, Singapore (Malay), Java, Borneo, Thailand, Laos, Myanmar, Bhutan, Bangladesh, India (Tripura, Ho, Konda Dora, Gond)
- O-M1283* Lao Isan[51]
- O-MF600645 Gansu (Hui,[41] Dongxiang[42]), Sichuan (Chengdu[42]), Hunan (Yiyang[42])
- O-M1368 Singapore[41]
- O-M1361
- O-MF611153 Found sporadically in China (Hunan, Hubei, Chongqing, Guangxi, Jiangxi[42])
- O-A22938 Vietnam (Kinh from Ho Chi Minh City[41]), China (Hong Kong,[41] Qinzhou,[42] Chongqing,[42] Lijiang[42])
- O-Y9322 China (Dai in Xishuangbanna,[41] Yunnan,[42] Chongqing,[42] Guangdong,[42] Sichuan,[42] etc.)
- O-Y9325
- O-Z39485 China (Dai, Yi)[41]
- O-Z39490
- O-Y9033/B426 Laos (Laotian[51]), Thailand (Blang,[51] Khmu,[51] Lawa,[51] Htin,[51] Padaung Karen,[51] Tai Dam,[51] Suay,[51] Khmer,[51] Mon,[51] Lao Isan,[51] Soa,[51] Shan,[51] Phutai,[51] Nyaw,[51] S'gaw Karen,[51] Thai,[51] Khon Mueang[51]), Vietnam (Mang from Mường Tè District,[45] Ede from Krông Buk District and Tuy An District,[45] Kinh from Hoàng Mai District, Gia Lâm District, and Yên Phong District,[45] Thái from Điện Biên Phủ,[45] Giarai from Ayun Pa[45])
- O-Y9325
- O-M1361
- O-F1252
- O-SK1630/F5504 China (esp. Sichuan and Guizhou, accounting for about 0.25% of the entire Chinese population[42])
- O-ACT5802
- O-MF92614
- O-F16061
- O-MF286118 Found in two Han Chinese from Guangdong[42]
- O-F19607
- O-ACT5802
- O-F2924
- O-CTS5854
- O-Z23810
- O-CTS7399
- O-Y85641 Japan (Tokyo[41]), China (esp. Shandong, Liaoning, Jilin, Heilongjiang[42])
- O-FGC19713/Y14026 Laos (Laotian in Vientiane and Luang Prabang[51]), Thailand (Tai Dam,[51] Tai Lue,[51] Nyah Kur,[51] Thai,[51] Eastern Lawa[51]), Vietnam (Thái from Bá Thước District and Tủa Chùa District,[45] Hà Nhì from Mường Tè District[45])
- O-FGC19707
- O-MF14427 China (esp. Jiangsu, Gansu, Henan, Shandong, Shanxi, Hebei, Shaanxi[42])
- O-FGC19716 China (Hong Kong,[41] Guangdong,[42] Hunan,[42] Chongqing[42])
- O-FGC19718 China (esp. Fujian, Jiangxi, Hubei, Jiangsu, Guangdong[42]), Philippines (Capiz[41])
- O-Z23849 China (Chongqing Han,[41] Xishuangbanna Dai,[41] Guangxi Zhuang,[41] Guangdong,[41] Shandong,[41] Tianjin[41])
- O-FGC19707
- O-CTS651/CTS10484 Thailand (Tai Khün,[51] Phuan,[51] Tai Lue,[51] Khon Mueang,[51] Eastern Lawa,[51] Lao Isan,[51] Thai[51]), Laos (Laotian in Vientiane[51]), Vietnam (Dao and Nùng from Hoàng Su Phì District,[45] Tày from Krông Pắk District, Hà Quảng District, and Đình Lập District[45])
- O-CTS7399
- O-Z23781 China (Henan[41])
- O-Z23810
- O-M111/M88 Found frequently among Vietnamese,[53][54][45] Tai peoples[55][56][54][45] (Bouyei,[55] Zhuang,[57][58][56] Nùng,[45] Tày,[45] Thái people in Vietnam,[45] Lao,[59] Northeastern Thai,[57] Northern Thai,[60][59] general population of Bangkok[54]), Lachi,[45] Lô Lô,[45] Hani-Akha,[55][54][45] Bunu,[61] She people,[53] Cambodians,[57] Kuy,[49][61] Bru,[61] and Htin,[49] with a moderate distribution among Qiang,[55] Bai,[62] Yi,[56] Bamar,[63] Jingpo,[63] Lahu,[45] Tujia,[57] Han Chinese,[57][55][53][54] Miao,[53][61] Pathen,[45] Yao,[55][53][61][45] Hlai,[57][55] Taiwanese aborigines[13][53][54] (especially Bunun[60][54]), the Philippines,[53][54] Malaysia[53] (Kota Kinabalu[13]), Kalimantan (Banjarmasin[13]), Java,[54] Chamic-speaking peoples (Cham from Bình Thuận,[59] Ede,[45] Jarai[45]), and Kiribati[60]
- O-M111/M88* Northern Thailand (Htin, Lawa), Cambodia (Jarai, Brao, Kachac, Khmer, Lao, Lun), Yunnan (De'ang)[49]
- O-F2524
- O-F2524* Jiangsu[41]
- O-F2346
- O-F2890 Thailand (Khon Mueang,[51] Phuan,[51] Shan,[51] Htin,[51] Tai Dam,[51] Thai,[51] Lawa,[51] Lao Isan,[51] Mon[51]), Vietnam (Kinh from Gia Lâm District,[45] Tày from Lục Yên District[45])
- O-F2890* Ho Chi Minh City[41]
- O-Z24048
- O-F2758 Vietnam (Kinh,[45] Lahu,[45] Dao, Pathen,[45] Tày,[45] Thái,[45] Ede,[45] Giarai[45]), Cambodia (Kuy, Tampuan, Khmer), Thailand (Phutai,[51] Bru,[51] Tai Khün,[51] Phuan,[51] Tai Dam,[51] Shan,[51] Khon Mueang,[51] Mon,[51] Lao Isan,[51] Tai Lue,[51] Htin,[49][51] Lawa,[49] Khmu,[51] Kaleun,[51] Nyaw,[51] Suay,[51] Thai[51]), Laos (Laotian in Luang Prabang[51]), Yunnan (Bulang, De'ang)[49]
- O-F2758* China (Miao,[41] Hunan[41])
- O-Z24083
- O-Z24083* Ho Chi Minh City (Kinh)
- O-Z24089
- O-SK1627/Z24091 Vietnam (Lô Lô from Mèo Vạc District,[45] La Chí and Nùng from Hoàng Su Phì District,[45] Hà Nhì from Mường Tè District,[45] Tày from Chợ Đồn District and Đăk Mil District,[45] Ede from Ea Kar District,[45] Kinh from Nghĩa Hưng District[45]), Thailand (Soa,[51] Saek,[51] Phutai,[51] Suay,[51] Tai Dam,[51] S'gaw Karen,[51] Nyah Kur,[51] Khmer,[51] Lawa,[51] Lao Isan,[51] Mon,[51] Thai[51]), Laos (Laotian in Vientiane[51])
- O-Z24091* China (Hebei,[41] Xishuangbanna Dai[41]), Vietnam (Kinh from Ho Chi Minh City[41])
- O-Y26364
- O-Y26364* Thailand (Phutai from Sakon Nakhon Province[51][41])
- O-Y26370 China (Tujia[41]), Vietnam (Kinh from Ho Chi Minh City[41])
- O-F923
- O-SK1627/Z24091 Vietnam (Lô Lô from Mèo Vạc District,[45] La Chí and Nùng from Hoàng Su Phì District,[45] Hà Nhì from Mường Tè District,[45] Tày from Chợ Đồn District and Đăk Mil District,[45] Ede from Ea Kar District,[45] Kinh from Nghĩa Hưng District[45]), Thailand (Soa,[51] Saek,[51] Phutai,[51] Suay,[51] Tai Dam,[51] S'gaw Karen,[51] Nyah Kur,[51] Khmer,[51] Lawa,[51] Lao Isan,[51] Mon,[51] Thai[51]), Laos (Laotian in Vientiane[51])
- O-F2890 Thailand (Khon Mueang,[51] Phuan,[51] Shan,[51] Htin,[51] Tai Dam,[51] Thai,[51] Lawa,[51] Lao Isan,[51] Mon[51]), Vietnam (Kinh from Gia Lâm District,[45] Tày from Lục Yên District[45])
- O-CTS5854
- O-SK1630/F5504 China (esp. Sichuan and Guizhou, accounting for about 0.25% of the entire Chinese population[42])
- O-CTS4040
- O-M176
- O-K4: Found frequently among Koreans and with a moderate distribution among Japanese, Ryukyuans, Daurs, Evenks, Hezhe, Manchus, and Sibe. Also found sporadically (<1%) among Han Chinese, Hui, Micronesians, Mongols, Thais, Uyghurs, Vietnamese, etc.
- O-47z: Found frequently among Japanese and Ryukyuans and with a moderate distribution among Koreans. Found sporadically (<1%) among Manchus, Mongols, Han Chinese, Hui, Tujia, Vietnamese, etc.
O-M122 (O2)
Found frequently among populations of East Asia, Southeast Asia, and culturally Austronesian regions of Oceania, with a moderate distribution in Central Asia (Shi 2005).
- O-M122
- O-CTS1754 East & Southeast Asia
- O-M324
- O-L465
- O-CTS727
- O-F915
- O-CTS3709
- O-JST002611/CTS2483
- O-CTS2483* China,[47] Japan,[47] Philippines[47]
- O-CTS10573 Beijing,[64] Sichuan,[64] Henan,[64] Jiangsu[64]
- O-F18
- O-CTS498 China,[41] Japan (Tokyo)[41]
- O-F449 Azerbaijan[47]
- O-F117
- O-F117* Fujian[41]
- O-F11
- O-F11* Gansu,[41] Japanese[41]
- O-F930 Beijing,[41] Armenia,[41] Inner Mongolia,[64] Hebei,[64] Shaanxi,[64] Shandong,[64] Zhejiang,[64] Hubei[64]
- O-F2685 Beijing, Shanghai, Fujian, Guangdong[64]
- O-BY169374
- O-F539 Beijing, Shanghai, Jiangsu, Zhejiang, Jiangxi, Guangdong, Yunnan[64]
- O-CTS12877
- O-Y29837
- O-BY36917 Japan[47]
- O-F4062 Beijing, Shanghai, Guangdong, Jiangsu, Shandong, Shaanxi, Chongqing, Heilongjiang, Liaoning, Henan, Hubei, Hunan, Zhejiang[64]
- O-Y15976 China, Japan,[47] Korea, Pakistan, Vietnam
- O-FGC54474
- O-F971 Beijing, Shanghai, Hubei, Guangdong[64]
- O-F632
- O-F632* Beijing[41]
- O-F16340 Zhejiang[41]
- O-F133 China, Bulgaria[47]
- O-CTS727
- O-P201
- O-M188
- O-M188* Korea[47]
- O-CTS800
- O-CTS445
- O-CTS201 Korea[47]
- O-M159 China (about 0.79% of the national male population[65]), Taiwan, Cambodia, Malaysia, Singapore[47]
- O-FTA21663/O-MF22947 China (Heilongjiang,[41][42] Inner Mongolia,[41][42] Zhejiang,[42] Shanghai,[42] Henan,[42] Hebei,[42] etc.; accounts for about 0.06% of the male population in China at present[66]), Saudi Arabia (al-Qaṣīm[41])
- O-CTS3994
- O-MF18110/FGC50590 China (esp. Guangdong, Zhejiang, Hunan, Shandong, and Guangxi[42])
- O-MF109844
- O-FGC50661 China (esp. Jiangsu and Hunan[42])
- O-MF56709
- O-FGC50643/MF15475 China (Shandong,[42] Hebei,[42] Hubei,[42] Shanxi,[41][42] Anhui,[42] Jiangsu,[42] etc.)
- O-MF56474 China (Jiangsu, Anhui, Jilin, Shandong, etc.[42])
- O-FGC50649
- O-Y169670/O-MF14256 China (esp. Jiangsu,[41][42] Shandong,[42] Zhejiang,[42] and Shanghai[42])
- O-MF50824
- O-MF14135/O-Z12303 China (currently accounts for about 0.44% of the total male population[68])
- O-MF238642
- O-MF37094 China (Zhejiang,[42] Jiangsu[42])
- O-Y169696/O-MF15693 China (Jiangsu,[41][42] Fufeng County,[42] Beijing,[42] Tangshan,[42] Feidong County,[42] Chifeng,[42] Xi County,[42] Min County,[42] Laizhou,[42] Rushan,[42] Harbin,[42] Yanji,[42] Dancheng County[42])
- O-MF18577/O-MF18626 China (currently accounts for about 0.23% of all males in China, especially in Jiangsu [1.08%], Shanghai [0.69%], Ningxia [0.39%], Shandong [0.38%], Anhui [0.33%], Heilongjiang [0.32%], Zhejiang [0.31%], and Jilin [0.26%][69]), Kazakhstan,[70] Thailand[70]
- O-MF238642
- O-FGC50558 Japan,[47] Korea[47]
- O-Y169670/O-MF14256 China (esp. Jiangsu,[41][42] Shandong,[42] Zhejiang,[42] and Shanghai[42])
- O-M159 China (about 0.79% of the national male population[65]), Taiwan, Cambodia, Malaysia, Singapore[47]
- O-M7 Found frequently among human remains associated with the Neolithic Daxi culture[71] and modern Hmong–Mien, Katuic, and Bahnaric peoples,[61] with a moderate distribution among Han Chinese (Xue 2006), Buyei (Xue 2006), Bai (Wen 2004), Mosuo (Wen 2004), Tibetans (Wen 2004), Qiang (Xue 2006), Oroqen (Xue 2006), Tujia (Su 2000), Thai (Su 2000), Orang Asli (Su 2000), western Indonesians (Su 2000 and Kayser 2008), Malaysians (Kayser 2008), Vietnamese (Kayser 2008), and Atayal (Su 2000).
- O-MF106687 China (Jinghu District,[42] etc.)
- O-Z25245
- O-MF9858/O-Z6157 China (approximately 0.08% of all males in present-day China[72]), Thailand (Central Thai in Central Thailand[51][43])
- O-Y26422
- O-F1276
- O-F1863
- O-MF107102 China (Tongchuan District[42])
- O-MF56735 China (Haiyan County, Suzhou, Wuxi, Shanghai, etc.[42])
- O-MF36531 China (Han in Yanping District[42])
- O-Y13816
- O-MF109664 China (Kazakh in Minqin County,[43] Kazakh in Tacheng City,[42] Han in Zizhong County,[42] Han in Furong District[42])
- O-MF36502 Guangdong (Kaiping, Yangjiang, Foshan, Lianjiang, etc.[42])
- O-Y13816
- O-F1134
- O-MF35799/O-Y94171 Thailand (Mon in Central Thailand[51][43]), China (observed sporadically in Pingyang County, Yunan County, Siming District, Longyao County, Shanwei, etc.[42])
- O-F1262/O-Y173492 China[41][70] (accounts for about 0.15% of the male population in China at present and is relatively concentrated in Zhejiang, Taiwan, Anhui, Jiangxi, etc.;[73] also observed in individuals from Zhenjiang,[43] Hejian,[43] and Langfang[43])
- O-FT303223/O-MF106843/O-F15314/O-F20756 China[70] (Changsha,[42] Chancheng District,[42] Wanzhou District,[42] Chaoyang District,[42] Dongying,[42] Chifeng,[42] Liaoyuan,[42] Harbin,[42] Han in Zhengzhou,[43] Dai in Xishuangbanna[41]), Thailand[70] (Khon Mueang in Northern Thailand,[51][43] Black Tai in Loei Province[51][43])
- O-Z25288/O-Z25293 Vietnam[70] (Kinh in Ho Chi Minh City,[41][43] Hanoi,[43] Nam Dinh,[43] and Lao Cai,[43] Giarai in Gia Lai,[43] Tày in Thai Nguyen[43])
- O-CTS6489
- O-MF106428/O-Y94472/O-FTB23660 Thailand[70] (Phayao,[41] Phutai, Lao Isan, Tai Lue, Phuan, Shan, Khon Mueang/Tai Yuan, Khmer, Mon[43]), Vietnam[70] (Tày in Lào Cai[43]), China (Dai in Xishuangbanna,[41] Achang in Yunnan;[43] accounts for about 0.05% of all males in China at present, mainly distributed in Guangxi and Guangdong[74])
- O-F1275 Guangxi (Dushan 4-1 ca. 7024 - 6643 BCE[70])
- O-MF15199/O-FTA25885
- O-F20472
- O-FTB23785 Thailand,[70] Vietnam[70]
- O-F17410/O-F18833/O-MF122643/O-BY177553 Thailand (Lao Isan in Northeast Thailand[51][43])
- O-MF106415/O-MF111486/O-BY122399 Thailand[70] (Shan in Mae Hong Son Province[75][43]), China (observed sporadically in individuals from Hubei, Hunan, Chongqing, Sichuan, Guangxi, Jiangxi, Zhejiang, Jiangsu, Anhui, Gansu, Shaanxi, Shanxi, Henan, and Shandong[42])
- O-Y127482/O-F15988 Thailand (Nyahkur and Lao Isan in Northeast Thailand[51][43])
- O-MF6534/O-MF58872/O-BY27925/O-Y23477 Thailand[70] (Central Thai in Central Thailand, Phuan in Central Thailand, Khon Mueang in North Thailand,[51][43] White Hmong in Chiang Rai Province[75][43]), Singapore,[41][43] China (Guangdong, Guangxi, Hunan, Sichuan, Jiangxi, Zhejiang, Shaanxi, Henan, Shandong[43][42])
- O-CTS6579
- O-CTS123/O-F22573/O-MF48275 China (Hunan Han;[41] accounts for about 0.13% of the male population in China at present, mainly distributed in Jiangxi, Hunan and other south-central provinces and cities[76])
- O-F14832/O-F15788/O-Y208219 China[70] (accounts for about 0.22% of the male population in China at present, mainly distributed in the northern region[77]), Thailand[70] (Mon in Western Thailand,[51][43] Tai Lue in Northern Thailand[51][43])
- O-F20472
- O-Z25411
- O-ACT1126/O-Y140772/O-F1289 China (relatively concentrated in northern China at present, accounting for about 0.24% of the national male population;[78] also found in Fujian[41]), Thailand[70] (Lisu[43])
- O-Z25398
- O-F22005/O-Z25400 Thailand[70] (Black Hmong in North Thailand[41][75]), Vietnam[70] (Kinh in Ho Chi Minh City[41]), China (currently distributed mainly in Guangxi, Sichuan, Guangdong and other places, accounting for about 0.10% of the national male population[79])
- O-F1100/O-Y37861 Hunan[41]
- O-MF17697 Laos,[70] Thailand,[70] China (Jiangsu, Hunan, Jiangxi, Guangxi, Guangdong, Guizhou, Yunnan, Fujian, Sichuan, Hong Kong, Chongqing, Henan, Liaoning[42])
- O-F1234/O-Y37855
- O-Y185160/O-MF36985 Hebei,[41] Beijing,[41] Sichuan, Shaanxi, Guangxi, Zhejiang, Shandong, Ningxia, Inner Mongolia, Hubei, Jiangxi (currently accounts for approximately 0.13% of the Chinese male population[80])
- O-FGC71370
- O-MF193618 Sichuan, Zhejiang, Shandong, Anhui, Hunan, Hubei, Fujian (currently accounts for about 0.08% of the male population in China, mainly distributed in Guangdong, Hunan, Anhui and other provinces and cities[81]), Philippines[70]
- O-F14904/N5 Ningxia,[41] Hmong (Northern Thailand[75]), She,[41] Iu Mien (Phayao Province[75]), Quebec[41]. Huang et al. (2022) found that this is the most common Y-chromosome haplogroup among many Hmongic-speaking ethnic groups (including Guangxi Miao, Hunan Miao, Hunan Pa-hng, and Thailand Hmong), with a frequency of 47.1% among the Guangxi Miao.[82]
- O-MF15199/O-FTA25885
- O-F1863
- O-CTS201 Korea[47]
- O-P164
- O-F996/F3237
- O-A16433 Heilongjiang[41]
- O-MF56976 Anhui[41]
- O-Y125645
- O-F871
- O-F706 Philippines, China, Cambodia,[47] Thailand (Bru in Sakon Nakhon Province[51])
- O-F1010 Thailand (Eastern Lawa, Blang, Palaung, Khon Mueang from Chiang Rai Province[51])
- O-AM01750/AM01861/B451 Singapore (Malay),[7] Indonesia (Bajo),[7] Philippines (Batak)[7]
- O-F2472
- O-F706 Philippines, China, Cambodia,[47] Thailand (Bru in Sakon Nakhon Province[51])
- O-A16433 Heilongjiang[41]
- O-M134: Found frequently among speakers of Sino-Tibetan languages, among members of the Kazakh Naiman tribe with a moderate distribution throughout East Asia and Southeast Asia.[citation needed]
- O-Y20/PAGES00125 Poland[47]
- O-F1725
- O-Y12/F314
- O-Y12* Beijing (Han)[41]
- O-CTS2643/CTS11192
- O-CTS53
- O-F876
- O-F275
- O-F634
- O-CTS3776/F2887
- O-M117/PAGE23
- O-MF1380/CTS4960 China, Korea, Japan,[47] Indonesia[47]
- O-M133/M1706 Shandong[41]
- O-M1706* Japan (Tokyo)[41]
- O-YP4864
- O-CTS7634
- O-M1726
- O-A9459
- O-F6800
- O-F14249
- O-F438 Japan (Tokyo)[41]
- O-CTS1642
- O-Y20/PAGES00125 Poland[47]
- O-F996/F3237
- O-M188
- O-L465
O-M324 (O2a)
[icon] | This section needs expansion. You can help by adding to it. (December 2017) |
O-F742 (O2b)
[icon] | This section needs expansion. You can help by adding to it. (December 2017) |
Language families and genes
Haplogroup O is associated with populations which speak Austric languages. The following is a phylogenetic tree of language families and their corresponding SNP markers, or haplogroups, sourced mainly from Edmondson 2007 and Shi 2005. This has been called the "Father Tongue Hypothesis" by George van Driem (van Driem 2011). It does not appear to account for O-M176, which is found among Japanese, Korean, and Manchurian males.
(M175) |
| ||||||||||||||||||
Phylogenetics
Phylogenetic history
Prior to 2002, there were in academic literature at least seven naming systems for the Y-Chromosome Phylogenetic tree. This led to considerable confusion. In 2002, the major research groups came together and formed the Y-Chromosome Consortium (YCC). They published a joint paper that created a single new tree that all agreed to use. Later, a group of citizen scientists with an interest in population genetics and genetic genealogy formed a working group to create an amateur tree aiming at being, above all, timely. The table below brings together all of these works at the point of the landmark 2002 YCC Tree. This allows a researcher reviewing older published literature to quickly move between nomenclatures.
YCC 2002/2008 (Shorthand) | (α) | (β) | (γ) | (δ) | (ε) | (ζ) | (η) | YCC 2002 (Longhand) | YCC 2005 (Longhand) | YCC 2008 (Longhand) | YCC 2010r (Longhand) | ISOGG 2006 | ISOGG 2007 | ISOGG 2008 | ISOGG 2009 | ISOGG 2010 | ISOGG 2011 | ISOGG 2012 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
O-M175 | 26 | VII | 1U | 28 | Eu16 | H9 | I | O* | O | O | O | O | O | O | O | O | O | O |
O-M119 | 26 | VII | 1U | 32 | Eu16 | H9 | H | O1* | O1a | O1a | O1a | O1a | O1a | O1a | O1a | O1a | O1a | O1a |
O-M101 | 26 | VII | 1U | 32 | Eu16 | H9 | H | O1a | O1a1 | O1a1a | O1a1a | O1a1 | O1a1 | O1a1a | O1a1a | O1a1a | O1a1a | O1a1a |
O-M50 | 26 | VII | 1U | 32 | Eu16 | H10 | H | O1b | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 | O1a2 |
O-P31 | 26 | VII | 1U | 33 | Eu16 | H5 | I | O2* | O2 | O2 | O2 | O2 | O2 | O2 | O2 | O2 | O2 | O2 |
O-M95 | 26 | VII | 1U | 34 | Eu16 | H11 | G | O2a* | O2a | O2a | O2a | O2a | O2a | O2a | O2a | O2a | O2a1 | O2a1 |
O-M88 | 26 | VII | 1U | 34 | Eu16 | H12 | G | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1 | O2a1a | O2a1a |
O-SRY465 | 20 | VII | 1U | 35 | Eu16 | H5 | I | O2b* | O2b | O2b | O2b | O2b | O2b | O2b | O2b | O2b | O2b | O2b |
O-47z | 5 | VII | 1U | 26 | Eu16 | H5 | I | O2b1 | O2b1a | O2b1 | O2b1 | O2b1a | O2b1a | O2b1 | O2b1 | O2b1 | O2b1 | O2b1 |
O-M122 | 26 | VII | 1U | 29 | Eu16 | H6 | L | O3* | O3 | O3 | O3 | O3 | O3 | O3 | O3 | O3 | O3 | O3 |
O-M121 | 26 | VII | 1U | 29 | Eu16 | H6 | L | O3a | O3a | O3a1 | O3a1 | O3a1 | O3a1 | O3a1 | O3a1 | O3a1 | O3a1a | O3a1a |
O-M164 | 26 | VII | 1U | 29 | Eu16 | H6 | L | O3b | O3b | O3a2 | O3a2 | O3a2 | O3a2 | O3a2 | O3a2 | O3a2 | O3a1b | O3a1b |
O-M159 | 13 | VII | 1U | 31 | Eu16 | H6 | L | O3c | O3c | O3a3a | O3a3a | O3a3 | O3a3 | O3a3a | O3a3a | O3a3a | O3a3a | O3a3a |
O-M7 | 26 | VII | 1U | 29 | Eu16 | H7 | L | O3d* | O3c | O3a3b | O3a3b | O3a4 | O3a4 | O3a3b | O3a3b | O3a3b | O3a2b | O3a2b |
O-M113 | 26 | VII | 1U | 29 | Eu16 | H7 | L | O3d1 | O3c1 | O3a3b1 | O3a3b1 | - | O3a4a | O3a3b1 | O3a3b1 | O3a3b1 | O3a2b1 | O3a2b1 |
O-M134 | 26 | VII | 1U | 30 | Eu16 | H8 | L | O3e* | O3d | O3a3c | O3a3c | O3a5 | O3a5 | O3a3c | O3a3c | O3a3c | O3a2c1 | O3a2c1 |
O-M117 | 26 | VII | 1U | 30 | Eu16 | H8 | L | O3e1* | O3d1 | O3a3c1 | O3a3c1 | O3a5a | O3a5a | O3a3c1 | O3a3c1 | O3a3c1 | O3a2c1a | O3a2c1a |
O-M162 | 26 | VII | 1U | 30 | Eu16 | H8 | L | O3e1a | O3d1a | O3a3c1a | O3a3c1a | O3a5a1 | O3a5a1 | O3a3c1a | O3a3c1a | O3a3c1a | O3a2c1a1 | O3a2c1a1 |
Original Research Publications
The following research teams per their publications were represented in the creation of the YCC Tree.
Phylogenetic trees
ISOGG 2017 tree (ver. 12.244).[86]
- O (M175)
- O1 (F265/M1354, CTS2866, F75/M1297, F429/M1415, F465/M1422)
- O1a (M119)
- O1a1 (B384/Z23193)
- O1a1a (M307.1/P203.1)
- O1a1a1 (F446)
- O1a1a1a (F140)
- O1a1a1a1 (F78)
- O1a1a1a1a (F81)
- O1a1a1a1a1 (CTS2458)
- O1a1a1a1a1a (F533)
- O1a1a1a1a1a1 (F492)
- O1a1a1a1a1a1a (F656)
- O1a1a1a1a1a1a1 (A12440)
- O1a1a1a1a1a1a1a (A12439)
- O1a1a1a1a1a1a2 (A14788)
- O1a1a1a1a1a1a3 (F65)
- O1a1a1a1a1a1a4 (MF1068)
- O1a1a1a1a1a1a5 (Z23482)
- O1a1a1a1a1a1a1 (A12440)
- O1a1a1a1a1a1b (FGC66168)
- O1a1a1a1a1a1b1 (CTS11553)
- O1a1a1a1a1a1c (Y31266)
- O1a1a1a1a1a1c1 (Y31261)
- O1a1a1a1a1a1d (A12441)
- O1a1a1a1a1a1e (MF1071)
- O1a1a1a1a1a1e1 (MF1074)
- O1a1a1a1a1a1a (F656)
- O1a1a1a1a1a2 (CTS4585)
- O1a1a1a1a1a1 (F492)
- O1a1a1a1a1a (F533)
- O1a1a1a1a2 (MF1075)
- O1a1a1a1a1 (CTS2458)
- O1a1a1a1a (F81)
- O1a1a1a2 (YP4610/Z39229)
- O1a1a1a2a (AM00330/AMM480/B386)
- O1a1a1a2a1 (AM00333/AMM483/B387)
- O1a1a1a2a1a (B388)
- O1a1a1a2a1 (AM00333/AMM483/B387)
- O1a1a1a2b (SK1555)
- O1a1a1a2a (AM00330/AMM480/B386)
- O1a1a1a1 (F78)
- O1a1a1b (SK1568/Z23420)
- O1a1a1b1 (M101)
- O1a1a1b2 (Z23392)
- O1a1a1b2a (Z23442)
- O1a1a1b2a1 (SK1571)
- O1a1a1b2a (Z23442)
- O1a1a1a (F140)
- O1a1a2 (CTS52)
- O1a1a2a (CTS701)
- O1a1a2a1 (K644/Z23266)
- O1a1a2a (CTS701)
- O1a1a1 (F446)
- O1a1b (CTS5726)
- O1a1a (M307.1/P203.1)
- O1a2 (M110)
- O1a2a (F3288)
- O1a2a1 (B392)
- O1a2a1a (B393)
- O1a2a1 (B392)
- O1a2a (F3288)
- O1a3 (Page109)
- O1a1 (B384/Z23193)
- O1b (M268)
- O1b1 (F2320)
- O1b1a (M1470)
- O1b1a1 (PK4)
- O1b1a1a (M95)
- O1b1a1a1 (F1803/M1348)
- O1b1a1a1a (F1252)
- O1b1a1a1a1 (F2924)
- O1b1a1a1a1a (M111)
- O1b1a1a1a1a1 (F2758)
- O1b1a1a1a1a1a (Z24083)
- O1b1a1a1a1a1a1 (Z24089)
- O1b1a1a1a1a1a1a (F923)
- O1b1a1a1a1a1a1a1 (CTS2022)
- O1b1a1a1a1a1a1a1a (F1399)
- O1b1a1a1a1a1a1a1a1 (F2415)
- O1b1a1a1a1a1a1a1a (F1399)
- O1b1a1a1a1a1a1a2 (Z24131)
- O1b1a1a1a1a1a1a3 (Z24100)
- O1b1a1a1a1a1a1a1 (CTS2022)
- O1b1a1a1a1a1a1b (SK1627/Z24091)
- O1b1a1a1a1a1a1b1 (Z39410)
- O1b1a1a1a1a1a1a (F923)
- O1b1a1a1a1a1a2 (Z24088)
- O1b1a1a1a1a1a1 (Z24089)
- O1b1a1a1a1a1a (Z24083)
- O1b1a1a1a1a2 (F2890)
- O1b1a1a1a1a2a (Z24048)
- O1b1a1a1a1a2a1 (Z24050)
- O1b1a1a1a1a2b (Z24014)
- O1b1a1a1a1a2a (Z24048)
- O1b1a1a1a1a1 (F2758)
- O1b1a1a1a1b (CTS5854)
- O1b1a1a1a1b1 (Z23810)
- O1b1a1a1a1b1a (CTS7399)
- O1b1a1a1a1b1a1 (FGC19713/Y14026)
- O1b1a1a1a1b1a1a (Z23849)
- O1b1a1a1a1b1a1a1 (FGC61038)
- O1b1a1a1a1b1a1a (Z23849)
- O1b1a1a1a1b1a1 (FGC19713/Y14026)
- O1b1a1a1a1b1b (CTS651)
- O1b1a1a1a1b1b1 (CTS9884)
- O1b1a1a1a1b1a (CTS7399)
- O1b1a1a1a1b2 (F4229)
- O1b1a1a1a1b2a (F809)
- O1b1a1a1a1b2a1 (F2517)
- O1b1a1a1a1b2a (F809)
- O1b1a1a1a1b1 (Z23810)
- O1b1a1a1a1a (M111)
- O1b1a1a1a2 (SK1630)
- O1b1a1a1a2a (SK1636)
- O1b1a1a1a1 (F2924)
- O1b1a1a1b (F789/M1283)
- O1b1a1a1b1 (FGC29900/Y9322/Z23667)
- O1b1a1a1b1a (B426/FGC29896/Y9033/Z23671)
- O1b1a1a1b1a1 (FGC29907/YP3930)
- O1b1a1a1b1a2 (B427/Z23680)
- O1b1a1a1b1b (Z39485)
- O1b1a1a1b1c (B418)
- O1b1a1a1b1a (B426/FGC29896/Y9033/Z23671)
- O1b1a1a1b2 (SK1646)
- O1b1a1a1b1 (FGC29900/Y9322/Z23667)
- O1b1a1a1a (F1252)
- O1b1a1a2 (CTS350)
- O1b1a1a3 (Page103)
- O1b1a1a1 (F1803/M1348)
- O1b1a1b (F838)
- O1b1a1b1 (F1199)
- O1b1a1a (M95)
- O1b1a2 (Page59)
- O1b1a2a (F993)
- O1b1a2a1 (F1759)
- O1b1a2a1a (CTS1127)
- O1b1a2a1 (F1759)
- O1b1a2b (F417/M1654)
- O1b1a2b1 (F840)
- O1b1a2b1a (F1127)
- O1b1a2b2 (CTS1451)
- O1b1a2b1 (F840)
- O1b1a2c (CTS9996)
- O1b1a2a (F993)
- O1b1a1 (PK4)
- O1b1a (M1470)
- O1b2 (P49, M176)
- O1b2a (F1942/Page92)
- O1b2a1 (CTS9259)
- O1b2a1a (F1204)
- O1b2a1a1 (CTS713)
- O1b2a1a1a (CTS1875)
- O1b2a1a1a1 (CTS10682)
- O1b2a1a1b (Z24598)
- O1b2a1a1c (CTS203)
- O1b2a1a1a (CTS1875)
- O1b2a1a2 (F2868)
- O1b2a1a2a (L682)
- O1b2a1a2a1 (CTS723)
- O1b2a1a2a1a (CTS7620)
- O1b2a1a2a1b (A12446)
- O1b2a1a2a1b1 (PH40)
- O1b2a1a2a1 (CTS723)
- O1b2a1a2b (F940)
- O1b2a1a2a (L682)
- O1b2a1a3 (CTS10687)
- O1b2a1a3a (CTS1215)
- O1b2a1a1 (CTS713)
- O1b2a1b (CTS562)
- O1b2a1a (F1204)
- O1b2a2 (Page90)
- O1b2a1 (CTS9259)
- O1b2a (F1942/Page92)
- O1b1 (F2320)
- O1a (M119)
- O2 (M122)
- O2a (M324)
- O2a1 (L127.1)
- O2a1a (F1876/Page127)
- O2a1a1 (F2159)
- O2a1a1a (F1867/Page124)
- O2a1a1a1 (F852)
- O2a1a1a1a (F2266)
- O2a1a1a1a1 (L599)
- O2a1a1a1a1a (Z43961)
- O2a1a1a1a1a1 (Z43963)
- O2a1a1a1a1a (Z43961)
- O2a1a1a1a1 (L599)
- O2a1a1a1b (F854)
- O2a1a1a1b1 (Z43966)
- O2a1a1a1c (Page130)
- O2a1a1a1a (F2266)
- O2a1a1a1 (F852)
- O2a1a1b (F915)
- O2a1a1b1 (F1478)
- O2a1a1b1a (PF5390)
- O2a1a1b1a1 (CTS1936)
- O2a1a1b1a1a (Z43975)
- O2a1a1b1a2 (FGC33994)
- O2a1a1b1a (PF5390)
- O2a1a1b1 (F1478)
- O2a1a1a (F1867/Page124)
- O2a1a1 (F2159)
- O2a1b (M164)
- O2a1c (IMS-JST002611)
- O2a1c1 (F18)
- O2a1c1a (F117)
- O2a1c1a1 (F13)
- O2a1c1a1a (F11)
- O2a1c1a1a1 (F632)
- O2a1c1a1a1a (F110/M11115)
- O2a1c1a1a1a1 (F17)
- O2a1c1a1a1a1a (F377)
- O2a1c1a1a1a1a1 (F1095)
- O2a1c1a1a1a1a1a (F856)
- O2a1c1a1a1a1a1a1 (F1418)
- O2a1c1a1a1a1a1a2 (Z25097)
- O2a1c1a1a1a1a1a (F856)
- O2a1c1a1a1a1a2 (CTS7501)
- O2a1c1a1a1a1a1 (F1095)
- O2a1c1a1a1a1b (F793)
- O2a1c1a1a1a1a (F377)
- O2a1c1a1a1a2 (Y20951)
- O2a1c1a1a1a2a (Y20932)
- O2a1c1a1a1a1 (F17)
- O2a1c1a1a1a (F110/M11115)
- O2a1c1a1a2 (F38)
- O2a1c1a1a3 (F12)
- O2a1c1a1a4 (F930)
- O2a1c1a1a4a (F2685)
- O2a1c1a1a5 (F1365/M5420/PF1558)
- O2a1c1a1a5a (Y15976)
- O2a1c1a1a5a1 (Y16154)
- O2a1c1a1a5a1a (Y26383)
- O2a1c1a1a5a1a1 (SK1686)
- O2a1c1a1a5a1a (Y26383)
- O2a1c1a1a5a1 (Y16154)
- O2a1c1a1a5b (FGC54486)
- O2a1c1a1a5b1 (FGC54507)
- O2a1c1a1a5a (Y15976)
- O2a1c1a1a6 (CTS12877)
- O2a1c1a1a6a (F2527)
- O2a1c1a1a6a1 (CTS5409)
- O2a1c1a1a6a2 (F2941)
- O2a1c1a1a6a (F2527)
- O2a1c1a1a7 (F723)
- O2a1c1a1a8 (CTS2107)
- O2a1c1a1a9 (SK1691)
- O2a1c1a1a1 (F632)
- O2a1c1a1b (PH203)
- O2a1c1a1a (F11)
- O2a1c1a1 (F13)
- O2a1c1b (F449)
- O2a1c1b1 (F238)
- O2a1c1b1a (F134)
- O2a1c1b1a1 (F1273)
- O2a1c1b1a2 (F724)
- O2a1c1b1a (F134)
- O2a1c1b2 (F1266)
- O2a1c1b1 (F238)
- O2a1c1c (CTS498)
- O2a1c1a (F117)
- O2a1c2 (FGC3750/SK1673)
- O2a1c1 (F18)
- O2a1a (F1876/Page127)
- O2a2 (IMS-JST021354/P201)
- O2a2a (M188)
- O2a2a1 (F2588)
- O2a2a1a (CTS445)
- O2a2a1a1 (CTS201)
- O2a2a1a1a (M159/Page96)
- O2a2a1a2 (M7)
- O2a2a1a2a (F1276)
- O2a2a1a2a1 (CTS6489)
- O2a2a1a2a1a (F1275)
- O2a2a1a2a1a1 (M113)
- O2a2a1a2a1a2 (N5)
- O2a2a1a2a1a3 (Z25400)
- O2a2a1a2a1a (F1275)
- O2a2a1a2a2 (F1863)
- O2a2a1a2a2a (F1134)
- O2a2a1a2a2a1 (F1262)
- O2a2a1a2a2a (F1134)
- O2a2a1a2a1 (CTS6489)
- O2a2a1a2b (Y26403)
- O2a2a1a2a (F1276)
- O2a2a1a1 (CTS201)
- O2a2a1b (F1837)
- O2a2a1a (CTS445)
- O2a2a2 (F879)
- O2a2a2a (F1226)
- O2a2a2a1 (F2859)
- O2a2a2a (F1226)
- O2a2a1 (F2588)
- O2a2b (P164)
- O2a2b1 (M134)
- O2a2b1a (F450/M1667)
- O2a2b1a1 (M117/Page23)
- O2a2b1a1a (M133)
- O2a2b1a1a1 (F438)
- O2a2b1a1a1a (Y17728)
- O2a2b1a1a1a1 (F155)
- O2a2b1a1a1a1a (F813/M6539)
- O2a2b1a1a1a1a1 (Y20928)
- O2a2b1a1a1a1a (F813/M6539)
- O2a2b1a1a1a2 (F1754)
- O2a2b1a1a1a2a (F2137)
- O2a2b1a1a1a2a1 (F1442)
- O2a2b1a1a1a2a1a (F1123)
- O2a2b1a1a1a2a1a1 (F1369)
- O2a2b1a1a1a2a1a (F1123)
- O2a2b1a1a1a2a2 (A16636)
- O2a2b1a1a1a2a1 (F1442)
- O2a2b1a1a1a2a (F2137)
- O2a2b1a1a1a3 (Z25907)
- O2a2b1a1a1a1 (F155)
- O2a2b1a1a1a (Y17728)
- O2a2b1a1a2 (FGC23469/Z25852)
- O2a2b1a1a2a (F310)
- O2a2b1a1a2a1 (F402)
- O2a2b1a1a2a1a (F1531)
- O2a2b1a1a2a1 (F402)
- O2a2b1a1a2a (F310)
- O2a2b1a1a3 (CTS7634)
- O2a2b1a1a3a (F317)
- O2a2b1a1a3a1 (F3039)
- O2a2b1a1a3a2 (Y29861)
- O2a2b1a1a3b (CTS5488)
- O2a2b1a1a3a (F317)
- O2a2b1a1a4 (Z25853)
- O2a2b1a1a4a (CTS5492)
- O2a2b1a1a4a1 (CTS6987)
- O2a2b1a1a4a1a (Z42620)
- O2a2b1a1a4a2 ( F20963)
- O2a2b1a1a4a1 (CTS6987)
- O2a2b1a1a4a (CTS5492)
- O2a2b1a1a5 (CTS10738/M1707)
- O2a2b1a1a5a (CTS9678)
- O2a2b1a1a5a1 (Z39663)
- O2a2b1a1a5a2 (M1513)
- O2a2b1a1a5b (A9457)
- O2a2b1a1a5b1 (F17158)
- O2a2b1a1a5a (CTS9678)
- O2a2b1a1a6 (CTS4658)
- O2a2b1a1a6a (CTS5308)
- O2a2b1a1a6b (Z25928)
- O2a2b1a1a6b1 (SK1730/Z25982)
- O2a2b1a1a6b1a (Z26030)
- O2a2b1a1a6b1b (Z26010)
- O2a2b1a1a6b2 (A9462)
- O2a2b1a1a6b3 (B456)
- O2a2b1a1a6b1 (SK1730/Z25982)
- O2a2b1a1a7 (YP4864)
- O2a2b1a1a7a (Z44068)
- O2a2b1a1a7a1 (F5525/SK1748)
- O2a2b1a1a7b (Z44071)
- O2a2b1a1a7a (Z44068)
- O2a2b1a1a8 (Z44091)
- O2a2b1a1a8a (Z44092)
- O2a2b1a1a1 (F438)
- O2a2b1a1b (CTS4960)
- O2a2b1a1a (M133)
- O2a2b1a2 (F114)
- O2a2b1a2a (F79)
- O2a2b1a2a1 (F46/Y15)
- O2a2b1a2a1a (FGC16847/Z26091)
- O2a2b1a2a1a1 (F48)
- O2a2b1a2a1a1a (F152)
- O2a2b1a2a1a1a1 (F2505)
- O2a2b1a2a1a1b (CTS3149)
- O2a2b1a2a1a1a (F152)
- O2a2b1a2a1a2 (F242)
- O2a2b1a2a1a2a (CTS4266)
- O2a2b1a2a1a2a1 (Z26108)
- O2a2b1a2a1a2a1a (F2173)
- O2a2b1a2a1a2a1 (Z26108)
- O2a2b1a2a1a2a (CTS4266)
- O2a2b1a2a1a3 (F2887)
- O2a2b1a2a1a3a (F3607)
- O2a2b1a2a1a3a1 (F3525)
- O2a2b1a2a1a3b (CTS3763)
- O2a2b1a2a1a3b1 (A9472)
- O2a2b1a2a1a3b2 (FGC16863/Y7110)
- O2a2b1a2a1a3b2a (L1360)
- O2a2b1a2a1a3b2a1 (FGC16889)
- O2a2b1a2a1a3b2b (SK1768/Y7112/Z26257)
- O2a2b1a2a1a3b2b1 (F4249)
- O2a2b1a2a1a3b2b1a (FGC23868)
- O2a2b1a2a1a3b2b2 (CTS335)
- O2a2b1a2a1a3b2b1 (F4249)
- O2a2b1a2a1a3b2a (L1360)
- O2a2b1a2a1a3a (F3607)
- O2a2b1a2a1a1 (F48)
- O2a2b1a2a1b (CTS53)
- O2a2b1a2a1b1 (CTS6373)
- O2a2b1a2a1b1a (A9473)
- O2a2b1a2a1b1 (CTS6373)
- O2a2b1a2a1c (F3386)
- O2a2b1a2a1d (Y29828)
- O2a2b1a2a1d1 (F735)
- O2a2b1a2a1d1a (FGC34973)
- O2a2b1a2a1d1b (F1739)
- O2a2b1a2a1d1 (F735)
- O2a2b1a2a1a (FGC16847/Z26091)
- O2a2b1a2a1 (F46/Y15)
- O2a2b1a2b (F743)
- O2a2b1a2b1 (CTS8481)
- O2a2b1a2b1a (CTS4325)
- O2a2b1a2b1a1 (A16629)
- O2a2b1a2b1a2 (CTS682)
- O2a2b1a2b1a (CTS4325)
- O2a2b1a2b2 (F748)
- O2a2b1a2b2a (F728)
- O2a2b1a2b1 (CTS8481)
- O2a2b1a2c (Page101)
- O2a2b1a2a (F79)
- O2a2b1a1 (M117/Page23)
- O2a2b1a (F450/M1667)
- O2a2b2 (AM01822/F3223)
- O2a2b2a (AM01856/F871)
- O2a2b2a1 (N7)
- O2a2b2a1a (F4110)
- O2a2b2a1a1 (F4068)
- O2a2b2a1a2 (SK1780)
- O2a2b2a1b (F4124)
- O2a2b2a1b1 (IMS-JST008425p6)
- O2a2b2a1b2 (BY15188)
- O2a2b2a1b2a (F16411)
- O2a2b2a1a (F4110)
- O2a2b2a2 (AM01845/F706)
- O2a2b2a2a (F717)
- O2a2b2a2a1 (F3612)
- O2a2b2a2a2 (SK1783)
- O2a2b2a2b (AM01847/B451)
- O2a2b2a2b1 (A17418)
- O2a2b2a2b2 (AM01756)
- O2a2b2a2b2a (B450)
- O2a2b2a2b2b (AM00472/B452)
- O2a2b2a2b2b1 (F18942)
- O2a2b2a2b2c (A16427)
- O2a2b2a2a (F717)
- O2a2b2a1 (N7)
- O2a2b2b (A16433)
- O2a2b2b1 (A16438)
- O2a2b2b1a (SK1775)
- O2a2b2b1a1 (SK1774)
- O2a2b2b1b (A16440)
- O2a2b2b1a (SK1775)
- O2a2b2b1 (A16438)
- O2a2b2a (AM01856/F871)
- O2a2b1 (M134)
- O2a2a (M188)
- O2a3 (M300)
- O2a4 (M333)
- O2a1 (L127.1)
- O2b (F742)
- O2b1 (F1150)
- O2b1a (F837)
- O2b1a1 (F1025)
- O2b1a (F837)
- O2b2 (F1055)
- O2b2a (F3021)
- O2b1 (F1150)
- O2a (M324)
- O1 (F265/M1354, CTS2866, F75/M1297, F429/M1415, F465/M1422)
See also
Genetics
Y-DNA O subclades
Y-DNA backbone tree
Notes
References
- ↑ 1.0 1.1 1.2 1.3 1.4 Monika Karmin, Rodrigo Flores, Lauri Saag, Georgi Hudjashov, Nicolas Brucato, Chelzie Crenna-Darusallam, Maximilian Larena, Phillip L Endicott, Mattias Jakobsson, J Stephen Lansing, Herawati Sudoyo, Matthew Leavesley, Mait Metspalu, François-Xavier Ricaut, and Murray P Cox, "Episodes of Diversification and Isolation in Island Southeast Asian and Near Oceanian Male Lineages," Molecular Biology and Evolution, Volume 39, Issue 3, March 2022, https://doi.org/10.1093/molbev/msac045
- ↑ 2.0 2.1 Poznik, G David; Xue, Yali; Mendez, Fernando L; Willems, Thomas F; Massaia, Andrea; Wilson Sayres, Melissa A; Ayub, Qasim; McCarthy, Shane A; Narechania, Apurva; Kashin, Seva; Chen, Yuan; Banerjee, Ruby; Rodriguez-Flores, Juan L; Cerezo, Maria; Shao, Haojing; Gymrek, Melissa; Malhotra, Ankit; Louzada, Sandra; Desalle, Rob; Ritchie, Graham R S; Cerveira, Eliza; Fitzgerald, Tomas W; Garrison, Erik; Marcketta, Anthony; Mittelman, David; Romanovitch, Mallory; Zhang, Chengsheng; Zheng-Bradley, Xiangqun; Abecasis, Gonçalo R; McCarroll, Steven A; Flicek, Paul; Underhill, Peter A; Coin, Lachlan; Zerbino, Daniel R; Yang, Fengtang; Lee, Charles; Clarke, Laura; Auton, Adam; Erlich, Yaniv; Handsaker, Robert E; Bustamante, Carlos D; Tyler-Smith, Chris; Tyler-Smith, C (June 2016). "Punctuated bursts in human male demography inferred from 1,244 worldwide Y-chromosome sequences". Nature Genetics. 48 (6): 593–599. doi:10.1038/ng.3559. PMC 4884158. PMID 27111036.
- ↑ ISOGG 2017
- ↑ 4.0 4.1 4.2 Ashirbekov, E. E.; Botbaev, D. M.; Belkozhaev, A. M.; Abayldaev, A. O.; Neupokoeva, A. S.; Mukhataev, J. E.; Alzhanuly, B.; Sharafutdinova, D. A.; Mukushkina, D. D.; Rakhymgozhin, M. B.; Khanseitova, A. K.; Limborska, S. A.; Aytkhozhina, N. A. (2017). "Distribution of Y-Chromosome Haplogroups of the Kazakh from the South Kazakhstan, Zhambyl, and Almaty Regions" (PDF). Reports of the National Academy of Sciences of the Republic of Kazakhstan. 6 (316): 85–95.
- ↑ Dulik MC, Osipova LP, Schurr TG (March 2011). "Y-chromosome variation in Altaian Kazakhs reveals a common paternal gene pool for Kazakhs and the influence of Mongolian expansions". PLOS ONE. 6 (3): e17548. Bibcode:2011PLoSO...617548D. doi:10.1371/journal.pone.0017548. PMC 3055870. PMID 21412412.
- ↑ 陆艳 [Lu Yan] (2011). 中国西部人群的遗传混合 [Genetic Mixture of Populations in Western China] (Thesis). Archived from the original on 27 March 2023. Retrieved 15 October 2021.
- ↑ 7.00 7.01 7.02 7.03 7.04 7.05 7.06 7.07 7.08 7.09 Karmin, Monika; et al. (April 2015). "A recent bottleneck of Y chromosome diversity coincides with a global change in culture". Genome Research. 25 (4): 459–466. doi:10.1101/gr.186684.114. PMC 4381518. PMID 25770088.
- ↑ 8.0 8.1 Yan, Shi; Wang, Chuan-Chao; Zheng, Hong-Xiang; Wang, Wei; Qin, Zhen-Dong; Wei, Lan-Hai; Wang, Yi; Pan, Xue-Dong; Fu, Wen-Qing; He, Yun-Gang; Xiong, Li-Jun; Jin, Wen-Fei; Li, Shi-Lin; An, Yu; Li, Hui; Jin, Li (29 August 2014). "Y Chromosomes of 40% Chinese Descend from Three Neolithic Super-Grandfathers". PLOS ONE. 9 (8): e105691. arXiv:1310.3897. Bibcode:2014PLoSO...9j5691Y. doi:10.1371/journal.pone.0105691. PMC 4149484. PMID 25170956.
- ↑ Maxat Zhabagin, Zhaxylyk Sabitov, Pavel Tarlykov, Inkar Tazhigulova, Zukhra Junissova, Dauren Yerezhepov, Rakhmetolla Akilzhanov, Elena Zholdybayeva, Lan-Hai Wei, Ainur Akilzhanova, Oleg Balanovsky, and Elena Balanovska, "The medieval Mongolian roots of Y-chromosomal lineages from South Kazakhstan." BMC Genetics 2020, 21(Suppl 1):87. https://doi.org/10.1186/s12863-020-00897-5
- ↑ Shou, Wei-Hua; Qiao, En-Fa; Wei, Chuan-Yu; Dong, Yong-Li; Tan, Si-Jie; Shi, Hong; Tang, Wen-Ru; Xiao, Chun-Jie (May 2010). "Y-chromosome distributions among populations in Northwest China identify significant contribution from Central Asian pastoralists and lesser influence of western Eurasians". Journal of Human Genetics. 55 (5): 314–322. doi:10.1038/jhg.2010.30. PMID 20414255. S2CID 23002493.
- ↑ Karafet, Tatiana M.; Mendez, Fernando L.; Sudoyo, Herawati; Lansing, J. Stephen; Hammer, Michael F. (March 2015). "Improved phylogenetic resolution and rapid diversification of Y-chromosome haplogroup K-M526 in Southeast Asia". European Journal of Human Genetics. 23 (3): 369–373. doi:10.1038/ejhg.2014.106. PMC 4326703. PMID 24896152.
- ↑ Msaidie S, Ducourneau A, Boetsch G, Longepied G, Papa K, Allibert C, et al. (January 2011). "Genetic diversity on the Comoros Islands shows early seafaring as major determinant of human biocultural evolution in the Western Indian Ocean". European Journal of Human Genetics. 19 (1): 89–94. doi:10.1038/ejhg.2010.128. PMC 3039498. PMID 20700146.
- ↑ 13.0 13.1 13.2 13.3 Hurles ME, Sykes BC, Jobling MA, Forster P (May 2005). "The dual origin of the Malagasy in Island Southeast Asia and East Africa: evidence from maternal and paternal lineages". American Journal of Human Genetics. 76 (5): 894–901. doi:10.1086/430051. PMC 1199379. PMID 15793703.
- ↑ Tofanelli S, Bertoncini S, Castrì L, Luiselli D, Calafell F, Donati G, Paoli G (September 2009). "On the origins and admixture of Malagasy: new evidence from high-resolution analyses of paternal and maternal lineages". Molecular Biology and Evolution. 26 (9): 2109–24. doi:10.1093/molbev/msp120. PMID 19535740.
- ↑ Cox MP, Mirazón Lahr M (January 2006). "Y-chromosome diversity is inversely associated with language affiliation in paired Austronesian- and Papuan-speaking communities from Solomon Islands". American Journal of Human Biology. 18 (1): 35–50. doi:10.1002/ajhb.20459. PMID 16378340.
- ↑ Malyarchuk B, Derenko M, Denisova G, Khoyt S, Woźniak M, Grzybowski T, Zakharov I (December 2013). "Y-chromosome diversity in the Kalmyks at the ethnical and tribal levels". Journal of Human Genetics. 58 (12): 804–11. doi:10.1038/jhg.2013.108. PMID 24132124.
- ↑ Har'kov VN, Hamina KV, Medvedeva OF, Simonova KV, Eremina ER, Stepanov VA (February 2014). "[Gene pool of Buryats: clinal variability and territorial subdivision based on data of Y-chromosome markers]". Genetika. 50 (2): 203–13. doi:10.1134/s1022795413110082. PMID 25711029. S2CID 15595963.
- ↑ Marchani EE, Watkins WS, Bulayeva K, Harpending HC, Jorde LB (July 2008). "Culture creates genetic structure in the Caucasus: autosomal, mitochondrial, and Y-chromosomal variation in Daghestan". BMC Genetics. 9: 47. doi:10.1186/1471-2156-9-47. PMC 2488347. PMID 18637195.
- ↑ Balanovsky, Oleg; Dibirova, Khadizhat; Dybo, Anna; Mudrak, Oleg; Frolova, Svetlana; Pocheshkhova, Elvira; Haber, Marc; Platt, Daniel; Schurr, Theodore; Haak, Wolfgang; Kuznetsova, Marina; Radzhabov, Magomed; Balaganskaya, Olga; Romanov, Alexey; Zakharova, Tatiana; Soria Hernanz, David F.; Zalloua, Pierre; Koshel, Sergey; Ruhlen, Merritt; Renfrew, Colin; Wells, R. Spencer; Tyler-Smith, Chris; Balanovska, Elena; Genographic, Consortium. (1 October 2011). "Parallel Evolution of Genes and Languages in the Caucasus Region". Molecular Biology and Evolution. 28 (10): 2905–2920. doi:10.1093/molbev/msr126. PMC 3355373. PMID 21571925.
- ↑ Haber, Marc; Platt, Daniel E.; Ashrafian Bonab, Maziar; Youhanna, Sonia C.; Soria-Hernanz, David F.; Martínez-Cruz, Begoña; Douaihy, Bouchra; Ghassibe-Sabbagh, Michella; Rafatpanah, Hoshang; Ghanbari, Mohsen; Whale, John; Balanovsky, Oleg; Wells, R. Spencer; Comas, David; Tyler-Smith, Chris; Zalloua, Pierre A. (28 March 2012). "Afghanistan's Ethnic Groups Share a Y-Chromosomal Heritage Structured by Historical Events". PLOS ONE. 7 (3): e34288. Bibcode:2012PLoSO...734288H. doi:10.1371/journal.pone.0034288. PMC 3314501. PMID 22470552.
- ↑ 21.0 21.1 Quintana-Murci L, Harmant C, Quach H, Balanovsky O, Zaporozhchenko V, Bormans C, et al. (April 2010). "Strong maternal Khoisan contribution to the South African coloured population: a case of gender-biased admixture". American Journal of Human Genetics. 86 (4): 611–20. doi:10.1016/j.ajhg.2010.02.014. PMC 2850426. PMID 20346436.
- ↑ Berniell-Lee, Gemma; Plaza, Stéphanie; Bosch, Elena; Calafell, Francesc; Jourdan, Eric; Césari, Maya; Lefranc, Gérard; Comas, David (May 2008). "Admixture and sexual bias in the population settlement of La Réunion Island (Indian Ocean)". American Journal of Physical Anthropology. 136 (1): 100–107. doi:10.1002/ajpa.20783. PMID 18186507.
- ↑ Simms TM, Wright MR, Hernandez M, Perez OA, Ramirez EC, Martinez E, Herrera RJ (August 2012). "Y-chromosomal diversity in Haiti and Jamaica: contrasting levels of sex-biased gene flow". American Journal of Physical Anthropology. 148 (4): 618–31. doi:10.1002/ajpa.22090. PMID 22576450.
- ↑ Mendizabal I, Sandoval K, Berniell-Lee G, Calafell F, Salas A, Martínez-Fuentes A, Comas D (July 2008). "Genetic origin, admixture, and asymmetry in maternal and paternal human lineages in Cuba". BMC Evolutionary Biology. 8 (1): 213. Bibcode:2008BMCEE...8..213M. doi:10.1186/1471-2148-8-213. PMC 2492877. PMID 18644108.
- ↑ Hammer, Michael F.; Chamberlain, Veronica F.; Kearney, Veronica F.; Stover, Daryn; Zhang, Gina; Karafet, Tatiana; Walsh, Bruce; Redd, Alan J. (December 2006). "Population structure of Y chromosome SNP haplogroups in the United States and forensic implications for constructing Y chromosome STR databases". Forensic Science International. 164 (1): 45–55. doi:10.1016/j.forsciint.2005.11.013. PMID 16337103.
- ↑ Stefflova, Klara; Dulik, Matthew C.; Pai, Athma A.; Walker, Amy H.; Zeigler-Johnson, Charnita M.; Gueye, Serigne M.; Schurr, Theodore G.; Rebbeck, Timothy R. (25 November 2009). "Evaluation of Group Genetic Ancestry of Populations from Philadelphia and Dakar in the Context of Sex-Biased Admixture in the Americas". PLOS ONE. 4 (11): e7842. Bibcode:2009PLoSO...4.7842S. doi:10.1371/journal.pone.0007842. PMC 2776971. PMID 19946364.
- ↑ Tariq, Muhammad; Ahmad, Habib; Hemphill, Brian E.; Farooq, Umar; Schurr, Theodore G. (2022). "Contrasting maternal and paternal genetic histories among five ethnic groups from Khyber Pakhtunkhwa, Pakistan". Scientific Reports. 12 (1027): 1027. Bibcode:2022NatSR..12.1027T. doi:10.1038/s41598-022-05076-3. PMC 8770644. PMID 35046511.
- ↑ Tariq, M.; Ahmad, H.; Hemphill, B. E.; Farooq, U.; Schurr, T. G. (2022). "Contrasting maternal and paternal genetic histories among five ethnic groups from Khyber Pakhtunkhwa, Pakistan". Scientific Reports. 12 (1): 1027. Bibcode:2022NatSR..12.1027T. doi:10.1038/s41598-022-05076-3. PMC 8770644. PMID 35046511.
- ↑ https://www.researchgate.net/publication/357933818_Contrasting_maternal_and_paternal_genetic_histories_among_five_ethnic_groups_from_Khyber_Pakhtunkhwa_Pakistan [bare URL]
- ↑ Tariq, Muhammad (2017). Genetic Analysis of the Major Tribes of Buner and Swabi Areas through Dental Morphology and DNA Analysis (This research study has been conducted and reported as partial fulfillment of the requirements of PhD degree in Genetics awarded by Hazara UniversityMansehra, Pakistan). Hazara University, Mansehra. pp. 1–229. Docket 13737.
- ↑ http://prr.hec.gov.pk/jspui/bitstream/123456789/9941/1/Muhammad%20Tariq_Genetics_2017_HU_Mansehra_Main%20part.pdf [bare URL PDF]
- ↑ Shou, Wei-Hua; Qiao, En-Fa; Wei, Chuan-Yu; Dong, Yong-Li; Tan, Si-Jie; Tang, Wen-Ru; Xiao, Chun-Jie (2010). "Y-chromosome distributions among populations in Northwest China identify significant contribution from Central Asian pastoralists and lesser influence of western Eurasians". Journal of Human Genetics. 55 (5): 314–322. doi:10.1038/jhg.2010.30. PMID 20414255.
- ↑ Shou, Wei-Hua; Qiao, En-Fa; Wei, Chuan-Yu; Dong, Yong-Li; Tan, Si-Jie; Shi, Hong; Tang, Wen-Ru; Xiao, Chun-Jie (2010). "Y-chromosome distributions among populations in Northwest China identify significant contribution from Central Asian pastoralists and lesser influence of western Eurasians". Journal of Human Genetics. 55 (5): 314–322. doi:10.1038/jhg.2010.30. PMID 20414255.
- ↑ Mehrjoo, Z; Fattahi, Z; Beheshtian, M; Mohseni, M; Poustchi, H; Ardalani, F (2019). "Distinct genetic variation and heterogeneity of the Iranian population". PLOS Genet. 15 (9): e1008385. doi:10.1371/journal.pgen.1008385. PMC 6759149. PMID 31550250.
- ↑ Fattahi, Z; Beheshtian, M; Mohseni, M (2019). "Iranome: A catalog of genomic variations in the Iranianpopulation". Human Mutation. 40 (11): 1968–1984. doi:10.1002/humu.23880. hdl:21.11116/0000-0004-DBEE-A. PMID 31343797.
- ↑ https://twitter.com/nrken19/status/1493354265548570627 [bare URL]
- ↑ https://twitter.com/nrken19/status/1529874531430563841 [bare URL]
- ↑ Wang, Chuan-Chao; Wang, Ling-Xiang; Shrestha, Rukesh; Zhang, Manfei; Huang, Xiu-Yuan; Hu, Kang; Jin, Li; Li, Hui (4 August 2014). Pereira, Luísa M. Sousa Mesquita (ed.). "Genetic Structure of Qiangic Populations Residing in the Western Sichuan Corridor". PLOS ONE. 9 (8): e103772. Bibcode:2014PLoSO...9j3772W. doi:10.1371/journal.pone.0103772. PMC 4121179. PMID 25090432.
- ↑ Di Cristofaro J, Pennarun E, Mazières S, Myres NM, Lin AA, Temori SA, et al. (2013). "Afghan Hindu Kush: where Eurasian sub-continent gene flows converge". PLOS ONE. 8 (10): e76748. Bibcode:2013PLoSO...876748D. doi:10.1371/journal.pone.0076748. PMC 3799995. PMID 24204668.
- ↑ Magoon, Gregory R.; Banks, Raymond H.; Rottensteiner, Christian; Schrack, Bonnie E.; Tilroe, Vincent O.; Robb, Terry; Grierson, Andrew J. (13 December 2013). "Generation of high-resolution a priori Y-chromosome phylogenies using 'next-generation' sequencing data". bioRxiv 10.1101/000802.S2CID 377800
- ↑ 41.000 41.001 41.002 41.003 41.004 41.005 41.006 41.007 41.008 41.009 41.010 41.011 41.012 41.013 41.014 41.015 41.016 41.017 41.018 41.019 41.020 41.021 41.022 41.023 41.024 41.025 41.026 41.027 41.028 41.029 41.030 41.031 41.032 41.033 41.034 41.035 41.036 41.037 41.038 41.039 41.040 41.041 41.042 41.043 41.044 41.045 41.046 41.047 41.048 41.049 41.050 41.051 41.052 41.053 41.054 41.055 41.056 41.057 41.058 41.059 41.060 41.061 41.062 41.063 41.064 41.065 41.066 41.067 41.068 41.069 41.070 41.071 41.072 41.073 41.074 41.075 41.076 41.077 41.078 41.079 41.080 41.081 41.082 41.083 41.084 41.085 41.086 41.087 41.088 41.089 41.090 41.091 41.092 41.093 41.094 41.095 41.096 41.097 41.098 41.099 41.100 41.101 41.102 41.103 41.104 41.105 41.106 41.107 41.108 41.109 41.110 41.111 41.112 41.113 41.114 41.115 41.116 41.117 41.118 41.119 41.120 41.121 41.122 41.123 41.124 41.125 41.126 41.127 41.128 41.129 41.130 41.131 41.132 41.133 41.134 41.135 41.136 41.137 41.138 41.139 41.140 41.141 41.142 41.143 41.144 41.145 41.146 41.147 41.148 41.149 41.150 41.151 41.152 41.153 41.154 41.155 41.156 41.157 41.158 41.159 41.160 41.161 41.162 41.163 41.164 41.165 41.166 41.167 41.168 41.169 41.170 41.171 41.172 41.173 41.174 41.175 41.176 41.177 41.178 41.179 41.180 41.181 41.182 41.183 41.184 41.185 41.186 41.187 41.188 41.189 41.190 41.191 41.192 41.193 41.194 41.195 41.196 41.197 41.198 41.199 41.200 41.201 41.202 41.203 41.204 41.205 41.206 41.207 41.208 41.209 41.210 41.211 41.212 41.213 41.214 41.215 41.216 41.217 41.218 41.219 41.220 41.221 41.222 41.223 41.224 41.225 41.226 41.227 41.228 41.229 41.230 41.231 41.232 41.233 41.234 41.235 41.236 41.237 41.238 41.239 41.240 41.241 41.242 41.243 41.244 41.245 41.246 41.247 41.248 41.249 41.250 41.251 41.252 41.253 41.254 41.255 41.256 41.257 41.258 41.259 41.260 41.261 41.262 41.263 41.264 41.265 41.266 41.267 41.268 41.269 41.270 41.271 41.272 41.273 41.274 41.275 41.276 41.277 41.278 41.279 41.280 41.281 41.282 41.283 41.284 41.285 41.286 41.287 41.288 41.289 41.290 41.291 41.292 41.293 41.294 41.295 41.296 41.297 41.298 41.299 41.300 41.301 41.302 41.303 41.304 41.305 41.306 41.307 41.308 41.309 41.310 41.311 41.312 41.313 41.314 41.315 41.316 41.317 41.318 41.319 41.320 41.321 41.322 41.323 41.324 41.325 41.326 41.327 41.328 41.329 41.330 41.331 41.332 41.333 41.334 41.335 41.336 41.337 41.338 41.339 41.340 41.341 41.342 41.343 41.344 41.345 41.346 41.347 41.348 41.349 41.350 41.351 41.352 41.353 41.354 41.355 41.356 41.357 41.358 41.359 41.360 41.361 41.362 41.363 41.364 41.365 41.366 41.367 41.368 41.369 41.370 41.371 41.372 41.373 41.374 41.375 41.376 41.377 41.378 41.379 41.380 41.381 41.382 41.383 41.384 41.385 41.386 41.387 41.388 41.389 41.390 41.391 41.392 41.393 41.394 41.395 41.396 41.397 41.398 41.399 41.400 41.401 41.402 41.403 41.404 41.405 41.406 41.407 41.408 41.409 41.410 41.411 41.412 41.413 41.414 41.415 41.416 41.417 41.418 41.419 41.420 41.421 41.422 41.423 41.424 41.425 41.426 41.427 41.428 41.429 41.430 41.431 41.432 41.433 41.434 41.435 41.436 41.437 41.438 41.439 41.440 41.441 41.442 41.443 41.444 41.445 41.446 41.447 41.448 41.449 41.450 41.451 41.452 YFull Haplogroup YTree v5.04 at 16 May 2017
- ↑ 42.000 42.001 42.002 42.003 42.004 42.005 42.006 42.007 42.008 42.009 42.010 42.011 42.012 42.013 42.014 42.015 42.016 42.017 42.018 42.019 42.020 42.021 42.022 42.023 42.024 42.025 42.026 42.027 42.028 42.029 42.030 42.031 42.032 42.033 42.034 42.035 42.036 42.037 42.038 42.039 42.040 42.041 42.042 42.043 42.044 42.045 42.046 42.047 42.048 42.049 42.050 42.051 42.052 42.053 42.054 42.055 42.056 42.057 42.058 42.059 42.060 42.061 42.062 42.063 42.064 42.065 42.066 42.067 42.068 42.069 42.070 42.071 42.072 42.073 42.074 42.075 42.076 42.077 42.078 42.079 42.080 42.081 42.082 42.083 42.084 42.085 42.086 42.087 42.088 42.089 42.090 42.091 42.092 42.093 42.094 42.095 42.096 42.097 42.098 42.099 42.100 42.101 42.102 42.103 42.104 42.105 42.106 42.107 42.108 42.109 42.110 42.111 42.112 42.113 42.114 42.115 42.116 42.117 42.118 42.119 42.120 42.121 42.122 42.123 42.124 42.125 42.126 42.127 42.128 42.129 42.130 42.131 42.132 42.133 42.134 42.135 42.136 42.137 42.138 42.139 42.140 42.141 42.142 42.143 42.144 42.145 42.146 Phylogenetic tree of Haplogroup O at 23mofang
- ↑ 43.00 43.01 43.02 43.03 43.04 43.05 43.06 43.07 43.08 43.09 43.10 43.11 43.12 43.13 43.14 43.15 43.16 43.17 43.18 43.19 43.20 43.21 43.22 43.23 43.24 43.25 43.26 43.27 43.28 43.29 43.30 43.31 43.32 43.33 43.34 43.35 43.36 43.37 43.38 43.39 43.40 43.41 Phylogenetic tree of Haplogroup O-F175 at TheYtree
- ↑ 44.0 44.1 Yan S, Wang CC, Li H, Li SL, Jin L, et al. (Genographic Consortium) (September 2011). "An updated tree of Y-chromosome Haplogroup O and revised phylogenetic positions of mutations P164 and PK4". European Journal of Human Genetics. 19 (9): 1013–5. doi:10.1038/ejhg.2011.64. PMC 3179364. PMID 21505448.
- ↑ 45.00 45.01 45.02 45.03 45.04 45.05 45.06 45.07 45.08 45.09 45.10 45.11 45.12 45.13 45.14 45.15 45.16 45.17 45.18 45.19 45.20 45.21 45.22 45.23 45.24 45.25 45.26 45.27 45.28 45.29 45.30 45.31 45.32 45.33 45.34 45.35 45.36 45.37 45.38 45.39 45.40 45.41 Macholdt, Enrico; Arias, Leonardo; Duong, Nguyen Thuy; Ton, Nguyen Dang; Van Phong, Nguyen; Schröder, Roland; Pakendorf, Brigitte; Van Hai, Nong; Stoneking, Mark (May 2020). "The paternal and maternal genetic history of Vietnamese populations". European Journal of Human Genetics. 28 (5): 636–645. doi:10.1038/s41431-019-0557-4. PMC 7171127. PMID 31827276.
- ↑ 46.0 46.1 O Y-Haplogroup Project at Family Tree DNA
- ↑ 47.00 47.01 47.02 47.03 47.04 47.05 47.06 47.07 47.08 47.09 47.10 47.11 47.12 47.13 47.14 47.15 47.16 47.17 47.18 47.19 47.20 47.21 47.22 47.23 47.24 47.25 47.26 47.27 47.28 47.29 47.30 47.31 Y-DNA Haplotree at Family Tree DNA
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- ↑ 49.0 49.1 49.2 49.3 49.4 49.5 49.6 49.7 49.8 Zhang, Xiaoming; Kampuansai, Jatupol; Qi, Xuebin; Yan, Shi; Yang, Zhaohui; Serey, Bun; Sovannary, Tuot; Bunnath, Long; Aun, Hong Seang; Samnom, Ham; Kutanan, Wibhu; Luo, Xin; Liao, Shiyu; Kangwanpong, Daoroong; Jin, Li; Shi, Hong; Su, Bing (27 June 2014). "An Updated Phylogeny of the Human Y-Chromosome Lineage O2a-M95 with Novel SNPs". PLOS ONE. 9 (6): e101020. Bibcode:2014PLoSO...9j1020Z. doi:10.1371/journal.pone.0101020. PMC 4074153. PMID 24972021.
- ↑ 50.0 50.1 Lippold, Sebastian; Xu, Hongyang; Ko, Albert; Li, Mingkun; Renaud, Gabriel; Butthof, Anne; Schröder, Roland; Stoneking, Mark (December 2014). "Human paternal and maternal demographic histories: insights from high-resolution Y chromosome and mtDNA sequences". Investigative Genetics. 5 (1): 13. doi:10.1186/2041-2223-5-13. PMC 4174254. PMID 25254093.
- ↑ 51.000 51.001 51.002 51.003 51.004 51.005 51.006 51.007 51.008 51.009 51.010 51.011 51.012 51.013 51.014 51.015 51.016 51.017 51.018 51.019 51.020 51.021 51.022 51.023 51.024 51.025 51.026 51.027 51.028 51.029 51.030 51.031 51.032 51.033 51.034 51.035 51.036 51.037 51.038 51.039 51.040 51.041 51.042 51.043 51.044 51.045 51.046 51.047 51.048 51.049 51.050 51.051 51.052 51.053 51.054 51.055 51.056 51.057 51.058 51.059 51.060 51.061 51.062 51.063 51.064 51.065 51.066 51.067 51.068 51.069 51.070 51.071 51.072 51.073 51.074 51.075 51.076 51.077 51.078 51.079 51.080 51.081 51.082 51.083 51.084 51.085 51.086 51.087 51.088 51.089 51.090 51.091 51.092 51.093 51.094 51.095 51.096 51.097 51.098 51.099 51.100 51.101 Kutanan, Wibhu; Kampuansai, Jatupol; Srikummool, Metawee; Brunelli, Andrea; Ghirotto, Silvia; Arias, Leonardo; Macholdt, Enrico; Hübner, Alexander; Schröder, Roland; Stoneking, Mark (1 July 2019). "Contrasting Paternal and Maternal Genetic Histories of Thai and Lao Populations". Molecular Biology and Evolution. 36 (7): 1490–1506. doi:10.1093/molbev/msz083. PMC 6573475. PMID 30980085.
- ↑ Xia, Zi-Yang; Yan, Shi; Wang, Chuan-Chao; Zheng, Hong-Xiang; Zhang, Fan; Liu, Yu-Chi; Yu, Ge; Yu, Bin-Xia; Shu, Li-Li; Jin, Li (9 August 2019). "Inland-coastal bifurcation of southern East Asians revealed by Hmong-Mien genomic history". bioRxiv 10.1101/730903.S2CID 202028061
- ↑ 53.0 53.1 53.2 53.3 53.4 53.5 53.6 53.7 Karafet, T. M.; Hallmark, B.; Cox, M. P.; Sudoyo, H.; Downey, S.; Lansing, J. S.; Hammer, M. F. (1 August 2010). "Major East-West Division Underlies Y Chromosome Stratification across Indonesia". Molecular Biology and Evolution. 27 (8): 1833–1844. doi:10.1093/molbev/msq063. PMID 20207712.
- ↑ 54.0 54.1 54.2 54.3 54.4 54.5 54.6 54.7 54.8 Trejaut, Jean A; Poloni, Estella S; Yen, Ju-Chen; Lai, Ying-Hui; Loo, Jun-Hun; Lee, Chien-Liang; He, Chun-Lin; Lin, Marie (2014). "Taiwan Y-chromosomal DNA variation and its relationship with Island Southeast Asia". BMC Genetics. 15 (1): 77. doi:10.1186/1471-2156-15-77. PMC 4083334. PMID 24965575.
- ↑ 55.0 55.1 55.2 55.3 55.4 55.5 55.6 Xue, Yali; Zerjal, Tatiana; Bao, Weidong; Zhu, Suling; Shu, Qunfang; Xu, Jiujin; Du, Ruofu; Fu, Songbin; Li, Pu; Hurles, Matthew E; Yang, Huanming; Tyler-Smith, Chris (1 April 2006). "Male Demography in East Asia: A North–South Contrast in Human Population Expansion Times". Genetics. 172 (4): 2431–2439. doi:10.1534/genetics.105.054270. PMC 1456369. PMID 16489223.
- ↑ 56.0 56.1 56.2 Hammer, Michael F.; Karafet, Tatiana M.; Park, Hwayong; Omoto, Keiichi; Harihara, Shinji; Stoneking, Mark; Horai, Satoshi (January 2006). "Dual origins of the Japanese: common ground for hunter-gatherer and farmer Y chromosomes". Journal of Human Genetics. 51 (1): 47–58. doi:10.1007/s10038-005-0322-0. PMID 16328082. S2CID 6559289.
- ↑ 57.0 57.1 57.2 57.3 57.4 57.5 Su, Bing; Xiao, Junhua; Underhill, Peter; Deka, Ranjan; Zhang, Weiling; Akey, Joshua; Huang, Wei; Shen, Di; Lu, Daru; Luo, Jingchun; Chu, Jiayou; Tan, Jiazhen; Shen, Peidong; Davis, Ron; Cavalli-Sforza, Luca; Chakraborty, Ranajit; Xiong, Momiao; Du, Ruofu; Oefner, Peter; Chen, Zhu; Jin, Li (December 1999). "Y-Chromosome Evidence for a Northward Migration of Modern Humans into Eastern Asia during the Last Ice Age". The American Journal of Human Genetics. 65 (6): 1718–1724. doi:10.1086/302680. PMC 1288383. PMID 10577926.
- ↑ Jing, Chen; Hui, Li; Zhen-Dong, Qin; Wen-Hong, Liu; Wei-Xiong, Lin; Rui-Xing, Yin; Li, Jin; Shang-Ling, Pan (December 2006). "Y-chromosome Genotyping and Genetic Structure of Zhuang Populations". Acta Genetica Sinica. 33 (12): 1060–1072. doi:10.1016/S0379-4172(06)60143-1. PMID 17185165.
- ↑ 59.0 59.1 59.2 He, Jun-Dong; Peng, Min-Sheng; Quang, Huy Ho; Dang, Khoa Pham; Trieu, An Vu; Wu, Shi-Fang; Jin, Jie-Qiong; Murphy, Robert W.; Yao, Yong-Gang; Zhang, Ya-Ping (7 May 2012). "Patrilineal Perspective on the Austronesian Diffusion in Mainland Southeast Asia". PLOS ONE. 7 (5): e36437. Bibcode:2012PLoSO...736437H. doi:10.1371/journal.pone.0036437. PMC 3346718. PMID 22586471.
- ↑ 60.0 60.1 60.2 Bing Su, Li Jin, Peter Underhill, et al. (2000), "Polynesian origins: Insights from the Y chromosome." PNAS, vol. 97, no. 15, 8225–8228.
- ↑ 61.0 61.1 61.2 61.3 61.4 61.5 Cai, Xiaoyun; Qin, Zhendong; Wen, Bo; Xu, Shuhua; Wang, Yi; Lu, Yan; Wei, Lanhai; Wang, Chuanchao; Li, Shilin; Huang, Xingqiu; Jin, Li; Li, Hui (31 August 2011). "Human Migration through Bottlenecks from Southeast Asia into East Asia during Last Glacial Maximum Revealed by Y Chromosomes". PLOS ONE. 6 (8): e24282. Bibcode:2011PLoSO...624282C. doi:10.1371/journal.pone.0024282. PMC 3164178. PMID 21904623.
- ↑ Wen, Bo (2004). "The origin of Mosuo people as revealed by mtDNA and Y chromosome variation". Science in China Series C. 47 (1): 1–10. doi:10.1360/02yc0207. PMID 15382670. S2CID 7999778.
- ↑ 63.0 63.1 Peng, Min-Sheng; He, Jun-Dong; Fan, Long; Liu, Jie; Adeola, Adeniyi C; Wu, Shi-Fang; Murphy, Robert W; Yao, Yong-Gang; Zhang, Ya-Ping (August 2014). "Retrieving Y chromosomal haplogroup trees using GWAS data". European Journal of Human Genetics. 22 (8): 1046–1050. doi:10.1038/ejhg.2013.272. PMC 4350590. PMID 24281365.
- ↑ 64.00 64.01 64.02 64.03 64.04 64.05 64.06 64.07 64.08 64.09 64.10 64.11 64.12 64.13 64.14 64.15 64.16 64.17 64.18 64.19 64.20 64.21 64.22 64.23 64.24 64.25 64.26 64.27 Yao X, Tang S, Bian B, Wu X, Chen G, Wang CC (April 2017). "Improved phylogenetic resolution for Y-chromosome Haplogroup O2a1c-002611". Scientific Reports. 7 (1): 1146. Bibcode:2017NatSR...7.1146Y. doi:10.1038/s41598-017-01340-z. PMC 5430735. PMID 28442769.
- ↑ "O-M159单倍群详情".
- ↑ "O-Mf22947单倍群详情".
- ↑ "O-Z25518单倍群详情".
- ↑ "O-Mf14135单倍群详情".
- ↑ "夏代东部大族祖源分析-23魔方祖源基因检测".
- ↑ 70.00 70.01 70.02 70.03 70.04 70.05 70.06 70.07 70.08 70.09 70.10 70.11 70.12 70.13 70.14 70.15 70.16 70.17 70.18 70.19 70.20 70.21 70.22 70.23 70.24 70.25 70.26 70.27 70.28 70.29 70.30 70.31 70.32 Time Tree of Y-DNA haplogroup O-M175 at FamilyTreeDNA Discover
- ↑ Li, Hui; Huang, Ying; Mustavich, Laura F.; Zhang, Fan; Tan, Jing-Ze; Wang, Ling-E; Qian, Ji; Gao, Meng-He; Jin, Li (November 2007). "Y chromosomes of prehistoric people along the Yangtze River". Human Genetics. 122 (3–4): 383–388. doi:10.1007/s00439-007-0407-2. PMID 17657509. S2CID 2533393.
- ↑ "O-Mf9858单倍群详情".
- ↑ "O-F1262单倍群详情".
- ↑ "O-Mf106428单倍群详情".
- ↑ 75.0 75.1 75.2 75.3 75.4 75.5 Kutanan, Wibhu; Shoocongdej, Rasmi; Srikummool, Metawee; Hübner, Alexander; Suttipai, Thanatip; Srithawong, Suparat; Kampuansai, Jatupol; Stoneking, Mark (November 2020). "Cultural variation impacts paternal and maternal genetic lineages of the Hmong-Mien and Sino-Tibetan groups from Thailand". European Journal of Human Genetics. 28 (11): 1563–1579. doi:10.1038/s41431-020-0693-x. PMC 7576213. PMID 32690935.
- ↑ "O-Mf48275单倍群详情".
- ↑ "O-F14832单倍群详情".
- ↑ "O-Y140772单倍群详情".
- ↑ "O-Z25400单倍群详情".
- ↑ "O-Mf36985单倍群详情".
- ↑ "O-Mf193618单倍群详情".
- ↑ Huang, Xiufeng; Xia, Zi-Yang; Bin, Xiaoyun; He, Guanglin; Guo, Jianxin (30 June 2022). "Genomic Insights Into the Demographic History of the Southern Chinese". Frontiers in Ecology and Evolution. 10. Frontiers Media SA. doi:10.3389/fevo.2022.853391. ISSN 2296-701X.
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- ↑ Wei, Lan-Hai; Yan, Shi; Teo, Yik-Ying; Huang, Yun-Zhi; Wang, Ling-Xiang; Yu, Ge; Saw, Woei-Yuh; Ong, Rick Twee-Hee; Lu, Yan; Zhang, Chao; Xu, Shu-Hua; Jin, Li; Li, Hui (5 April 2017). "Phylogeography of Y-chromosome haplogroup O3a2b2-N6 reveals patrilineal traces of Austronesian populations on the eastern coastal regions of Asia". PLOS ONE. 12 (4): e0175080. Bibcode:2017PLoSO..1275080W. doi:10.1371/journal.pone.0175080. PMC 5381892. PMID 28380021.
- ↑ 85.0 85.1 85.2 85.3 Mondal, Mayukh; Casals, Ferran; Xu, Tina; Dall'Olio, Giovanni M; Pybus, Marc; Netea, Mihai G; Comas, David; Laayouni, Hafid; Li, Qibin; Majumder, Partha P; Bertranpetit, Jaume (September 2016). "Genomic analysis of Andamanese provides insights into ancient human migration into Asia and adaptation". Nature Genetics. 48 (9): 1066–1070. doi:10.1038/ng.3621. hdl:10230/34401. PMID 27455350. S2CID 205352099.
- ↑ "Y-DNA Haplogroup D-M174 and its Subclades - 2017".
Sources for conversion tables
- Capelli, Cristian; Wilson, James F.; Richards, Martin; Stumpf, Michael P.H.; et al. (February 2001). "A Predominantly Indigenous Paternal Heritage for the Austronesian-Speaking Peoples of Insular Southeast Asia and Oceania". The American Journal of Human Genetics. 68 (2): 432–443. doi:10.1086/318205. PMC 1235276. PMID 11170891.
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Further reading
- Edmondson JA (2007). Jimmy G. Harris, Somsonge Burusphat and James E. Harris (ed.). "The power of language over the past: Tai settlement and Tai linguistics in southern China and northern Vietnam" (PDF). Studies in Southeast Asian Languages and Linguistics. Bangkok, Thailand: Ek Phim Thai Co. Ltd. Archived from the original (PDF) on 21 August 2007. Retrieved 24 October 2010.
- van Driem, George (2011). "Rice and the Austroasiatic and Hmong-Mien Homelands". In Enfield, N. J (ed.). Dynamics of Human Diversity (PDF). Pacific Linguistics. pp. 361–390. CiteSeerX 10.1.1.694.9991. ISBN 978-0-85883-638-9. S2CID 135246934. Archived from the original on 7 February 2016.
{{cite book}}
: CS1 maint: unfit URL (link) - Firasat S, Khaliq S, Mohyuddin A, Papaioannou M, Tyler-Smith C, Underhill PA, Ayub Q (January 2007). "Y-chromosomal evidence for a limited Greek contribution to the Pathan population of Pakistan". European Journal of Human Genetics. 15 (1): 121–6. doi:10.1038/sj.ejhg.5201726. PMC 2588664. PMID 17047675.
- Fornarino, Simona; Pala, Maria; Battaglia, Vincenza; Maranta, Ramona; Achilli, Alessandro; Modiano, Guido; Torroni, Antonio; Semino, Ornella; Santachiara-Benerecetti, Silvana A (December 2009). "Mitochondrial and Y-chromosome diversity of the Tharus (Nepal): a reservoir of genetic variation". BMC Evolutionary Biology. 9 (1): 154. Bibcode:2009BMCEE...9..154F. doi:10.1186/1471-2148-9-154. PMC 2720951. PMID 19573232.
- Karafet TM, Mendez FL, Meilerman MB, Underhill PA, Zegura SL, Hammer MF (May 2008). "New binary polymorphisms reshape and increase resolution of the human Y chromosomal haplogroup tree". Genome Research. 18 (5): 830–8. doi:10.1101/gr.7172008. PMC 2336805. PMID 18385274.
- Kayser M, Choi Y, van Oven M, Mona S, Brauer S, Trent RJ, et al. (July 2008). "The impact of the Austronesian expansion: evidence from mtDNA and Y chromosome diversity in the Admiralty Islands of Melanesia". Molecular Biology and Evolution. 25 (7): 1362–74. doi:10.1093/molbev/msn078. PMID 18390477.
- Kharkov, V. N.; Stepanov, V. A.; Medvedeva, O. F.; Spiridonova, M. G.; Voevoda, M. I.; Tadinova, V. N.; Puzyrev, V. P. (2007). "Gene pool differences between Northern and Southern Altaians inferred from the data on Y-chromosomal haplogroups". Russian Journal of Genetics. 43 (5): 551–562. doi:10.1134/S1022795407050110. PMID 17633562. S2CID 566825.
- Kim SH, Kim KC, Shin DJ, Jin HJ, Kwak KD, Han MS, et al. (April 2011). "High frequencies of Y-chromosome haplogroup O2b-SRY465 lineages in Korea: a genetic perspective on the peopling of Korea". Investigative Genetics. 2 (1): 10. doi:10.1186/2041-2223-2-10. PMC 3087676. PMID 21463511.
- Ratliff M (1998). "Ho Ne (She) is Hmongic: One final argument" (PDF). Linguistics of the Tibeto-Burman Area. 21 (2): 97–109.
- Rootsi S, Zhivotovsky LA, Baldovic M, Kayser M, Kutuev IA, Khusainova R, et al. (February 2007). "A counter-clockwise northern route of the Y-chromosome haplogroup N from Southeast Asia towards Europe". European Journal of Human Genetics. 15 (2): 204–11. doi:10.1038/sj.ejhg.5201748. PMID 17149388.
- Scheinfeldt L, Friedlaender F, Friedlaender J, Latham K, Koki G, Karafet T, et al. (August 2006). "Unexpected NRY chromosome variation in Northern Island Melanesia". Molecular Biology and Evolution. 23 (8): 1628–41. doi:10.1093/molbev/msl028. PMID 16754639.
- Shi H, Dong YL, Wen B, Xiao CJ, Underhill PA, Shen PD, et al. (September 2005). "Y-chromosome evidence of southern origin of the East Asian-specific haplogroup O3-M122". American Journal of Human Genetics. 77 (3): 408–19. doi:10.1086/444436. PMC 1226206. PMID 16080116.
- Su B, Jin L, Underhill P, Martinson J, Saha N, McGarvey ST, et al. (July 2000). "Polynesian origins: insights from the Y chromosome". Proceedings of the National Academy of Sciences of the United States of America. 97 (15): 8225–8. Bibcode:2000PNAS...97.8225S. doi:10.1073/pnas.97.15.8225. PMC 26928. PMID 10899994.
- Wells RS, Yuldasheva N, Ruzibakiev R, Underhill PA, Evseeva I, Blue-Smith J, et al. (August 2001). "The Eurasian heartland: a continental perspective on Y-chromosome diversity". Proceedings of the National Academy of Sciences of the United States of America. 98 (18): 10244–9. Bibcode:2001PNAS...9810244W. doi:10.1073/pnas.171305098. PMC 56946. PMID 11526236.
- Bo W, Hong S, Ling R, Huifeng X, Kaiyuan L, Wenyi Z, et al. (February 2004). "The origin of Mosuo people as revealed by mtDNA and Y chromosome variation". Science in China Series C: Life Sciences. 47 (1): 1–10. doi:10.1360/02yc0207. PMID 15382670. S2CID 7999778.
- Xue Y, Zerjal T, Bao W, Zhu S, Shu Q, Xu J, et al. (April 2006). "Male demography in East Asia: a north-south contrast in human population expansion times". Genetics. 172 (4): 2431–9. doi:10.1534/genetics.105.054270. PMC 1456369. PMID 16489223.
External links
- Bradshaw Foundation. "Journey of Man - The Peopling of the World".
- ISOGG (2012). "Y-DNA Haplogroup O and its Subclades - 2012".
- TMC (1998). "Genetic Findings Support 'Out of Africa' Theory". Archived from the original on 10 October 2009.
- Spread of Haplogroup O, from The Genographic Project, National Geographic
- Y-DNA Phylogenetic Tree of Haplogroup O (DNAHaplogroups.org)
- Migration patterns of early Humans and the full size map
- China DNA at Family Tree DNA