A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678069



Internal ID9944174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:66585478..66585834hg38UCSC Ensembl
Outerchr15:66585107..66586254hg38UCSC Ensembl
Innerchr15:66877816..66878172hg19UCSC Ensembl
Outerchr15:66877445..66878592hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381148
hg191148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv456e199
Supporting Variantsessv6483394, essv6411970, essv6049014, essv6022189, essv5791052, essv6425862, essv6162953, essv5407129, essv6248981, essv6341775, essv5473872, essv5701988, essv5417697, essv6572246, essv6228194, essv5929684, essv6356473, essv5673912, essv5525649, essv6074037, essv5404350, essv6197297, essv6042420, essv6402405, essv6413615, essv5983848, essv5787586, essv6341660, essv5473230, essv6539576, essv5502356, essv5685903, essv6177575, essv5614300, essv5778938, essv5857314, essv5684138, essv5784433, essv5941123, essv6038690, essv5479263, essv5697823, essv5397369, essv6473349, essv6055245, essv5653486, essv5536646, essv5994494, essv5488200, essv5827876, essv5605650, essv6338229, essv5542917, essv6514272, essv5464540, essv5399923, essv6242132, essv6328765, essv5869866, essv5726350, essv5822800, essv5753300, essv6543564, essv5927467, essv5899043, essv6103531, essv5983359, essv6348774, essv6234753, essv5678977, essv6577834, essv6543421, essv5612523, essv6565195, essv5468315, essv5709133, essv6180134, essv5693106, essv6520013, essv5490583, essv5635746, essv6222829, essv5583546, essv5521873, essv5914994, essv5897990, essv5432160, essv5968102, essv5553235, essv6306375, essv5556496, essv5542981, essv6157173, essv6360135, essv6408803, essv6190826, essv5610225, essv6133540, essv5885093, essv6598055, essv6319247, essv6567325, essv6102985, essv6584569, essv6059099, essv5969316, essv6423201, essv5964862, essv5978674, essv6037167, essv6066928, essv5666223, essv6538141, essv5426115, essv6264474, essv6581334, essv6317355, essv6083162, essv6404636, essv5547307, essv5468821, essv6259083, essv5766094, essv6302564, essv6261927, essv6050711, essv5422494, essv5756044, essv6240867, essv5445245, essv6360605, essv6414928, essv6563834, essv5770575, essv5908666, essv6197677, essv6318471, essv6531780, essv5760760, essv6502026, essv6415511, essv5789005, essv6548401, essv6487269, essv6316210, essv6288504, essv6596114, essv5864211, essv5688595, essv5604780, essv6216036, essv6597766, essv6090123, essv5917657, essv5943433, essv6033960, essv6460269
SamplesNA20588, NA12383, HG01060, NA11830, NA19700, HG01098, HG01356, HG00231, HG01462, NA12286, HG00249, NA11995, NA10851, NA12273, NA12414, HG01079, HG00100, NA11933, NA11931, HG00257, HG01389, HG01374, NA12751, HG01465, NA12340, HG01456, NA12058, HG00115, HG00150, NA12400, HG00261, NA12413, NA12341, HG00641, HG00138, HG01350, NA19379, HG00251, HG01351, HG01488, NA11992, NA07347, NA12283, HG01354, NA12287, HG00247, HG00369, HG01365, NA20513, HG00243, HG00158, NA12761, HG00139, NA12282, NA12275, HG01455, HG00335, HG00148, HG00106, NA12156, HG01170, HG00236, HG00156, HG01495, NA11932, NA12044, HG01440, HG00160, HG00118, NA19725, HG00159, HG01133, NA19789, NA12748, NA11993, HG00464, HG01124, NA11831, HG00137, HG00133, HG00149, HG01360, HG00282, HG01384, NA12003, HG01498, NA12718, NA20519, HG00740, HG01390, HG01073, NA11919, HG00651, HG00373, HG00479, NA12829, NA11893, HG01197, NA11894, NA18856, NA12249, HG00117, HG00157, NA18853, NA12827, HG01334, HG00152, HG00146, NA12144, NA12778, HG00246, HG00126, NA12043, HG01148, HG00258, NA19652, HG00155, NA20801, HG00254, HG00119, NA19390, NA11881, NA12775, NA19072, HG01253, NA07051, HG01357, HG01375, HG01494, NA19311, HG01113, HG00116, NA07037, NA19783, NA18615, HG01342, NA12347, HG00339, HG00125, NA19785, NA12749, HG00174, HG00123, NA12830, HG00112, NA20758, HG00377, HG00372, HG01377, HG01378, NA19755, HG01125, NA12006, NA07000, NA12154, HG00553, NA12776
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678069
Frequency
Sample Size1151
Observed Gain0
Observed Loss157
Observed Complex0
Frequencyn/a


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