AU73560
古人
hg19 / GRCh37
X2b-T226C
K47
伏尔加 Volgan: 22.77%
北伊比利亚 North-Iberian: 17.31%
凯尔特人 Celtic: 14.90%
亚马逊 Amazonian: 13.35%
斯堪的纳维亚-日耳曼 Scando-Germanic: 11.47%
东伊比利亚 East-Iberian: 9.27%
西芬兰 West-Finnic: 6.14%
西地中海 West-Med: 4.79%

MichalK25
东北欧 Northeast European: 43.57%
地中海 Mediterranean: 30.35%
南美印第安人 South Amerindian: 20.55%
西伯利亚 Siberian: 5.53%

K12b
北欧 North European: 55.00%
西南亚 Southwest Asian: 18.99%
大西洋地中海 Atlantic Med: 17.82%
西伯利亚 Siberian: 8.19%

puntDNAL
新石器时代伊朗 Iran Neolithic: 36.52%
美洲印第安人 Amerinidian: 27.97%
纳吐夫狩猎采集者 Natufian HG: 24.70%
欧洲狩猎采集者-大草原 EHG-Steppe: 4.66%
西方狩猎采集者 Western HG: 3.30%
西伯利亚 Siberian: 2.86%

AncientNearEast13
高加索狩猎采集者-早期欧洲农人 CHG-EEF: 67.60%
欧洲狩猎采集者 EHG: 17.92%
斯堪的纳维亚-西欧狩猎采集者 SHG-WHG: 9.27%
新石器时代伊朗 Iran-Neolithic: 3.61%
纳吐夫 Natufian: 1.60%
Finland
Site Helsinki
Diagnosis: Trisomy 21 Age at death: Full-term Osteological possible diagnosis: Vitamin C deficiency
1667–1800 CEb
Cases of trisomy 21 and trisomy 18 among historic and prehistoric individuals discovered from ancient DNA


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HKI002/Grave 13 - 1667–1800 CEb - 祖源树TheYtree 祖源树, 父系树