A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672564



Internal ID9938669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23122555..23122995hg38UCSC Ensembl
chr20:23103192..23103632hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38441
hg19441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv782e199
Supporting Variantsessv6373670, essv5505554, essv5722161, essv5559066, essv6012161, essv6109724, essv5776413, essv5797034, essv5633791, essv5856822, essv5898668, essv5807394, essv5912334, essv5605445, essv6024684, essv6286434, essv5549574, essv6280761, essv5906262, essv5757264, essv5560347, essv6042681, essv5408484, essv6271935, essv5592133, essv5556125, essv6269437, essv6061752, essv5669245, essv6105031, essv5542945, essv5813540, essv6081576, essv5719536, essv5454740, essv6067357, essv5917665, essv5827571, essv5802767, essv6510519, essv5559203, essv5517233, essv5931565, essv5896604, essv5761642, essv5413827, essv5395698, essv5534991, essv5949158, essv5842278, essv5697985, essv6453101, essv6353638, essv5443331, essv6289983, essv6471594, essv6390540, essv5649840, essv6270060, essv6246927, essv5756628, essv5944073, essv6512011, essv6469926, essv5979507, essv6412702, essv6050961, essv6353428, essv6356233, essv6415051, essv5593417, essv6314812, essv6111823, essv5897168, essv5424381, essv5434943, essv6184990, essv6135650, essv6065003, essv5448303, essv5701060, essv5923114, essv6462918, essv6403989, essv5929719, essv5933493, essv5559507, essv5555260, essv6063797, essv5666538, essv6056837, essv5735798, essv5936594, essv5704407, essv6260497, essv6228494, essv5565376, essv5691594, essv6152506, essv6344286, essv5999360, essv5741170, essv5582174, essv6515476, essv5548055, essv6400325, essv6174632, essv6058815, essv5902854, essv6187143, essv5685890, essv5475053, essv5551986, essv5437201, essv6322623, essv6112854, essv5499269, essv6044718, essv5439599, essv6589516, essv5680630, essv5546754, essv6244106, essv6209267, essv5724043, essv5932084, essv5844950, essv5519174, essv5524616, essv5874999, essv6589512, essv5836685, essv6313925, essv6058217, essv5968370, essv5696537, essv6209729, essv5757410, essv6394091, essv5841849, essv6325869, essv6452072, essv6024555, essv6256543, essv6205956, essv5529961, essv6321116, essv5696000, essv6095320, essv6017475, essv5453594, essv5499279, essv6009603, essv5816418, essv5793988, essv6082516, essv6245206, essv6336340, essv5564556, essv5482375, essv6175013, essv6502828, essv6314053, essv5805454, essv6157305, essv5615195, essv6473284, essv5703404, essv5689659, essv5471630, essv5412923, essv5963064, essv6160707, essv6207887, essv5707597, essv6477867, essv6330085, essv6225409, essv6501515, essv6509807, essv5934151, essv6297491, essv5580900, essv5746597, essv6436471, essv6275325, essv5963357, essv6199535, essv5556677, essv5909996, essv6259574, essv5972456, essv5703316, essv6467433, essv5873199, essv5714738, essv6249882, essv5702031, essv6354364, essv5715082, essv5923625, essv5943243, essv5643441, essv6231631, essv5939950, essv5635204, essv6127969, essv6537624, essv6344690, essv5692929, essv6173072, essv6417476, essv6239901, essv5781142, essv5649679, essv6491388, essv5995763, essv5588448, essv6183621, essv5949872, essv5931010
SamplesHG00189, NA20761, NA19648, NA19700, NA19058, HG01098, NA18924, HG00142, NA19664, NA19466, NA11829, HG00361, NA19066, HG00242, HG00559, HG00187, NA20514, HG00306, HG00151, NA20816, NA20813, NA20802, NA12045, HG00244, NA19092, HG01465, NA18545, NA19819, NA19777, NA19684, NA12058, HG00179, HG00115, NA20808, NA20507, NA19443, NA19920, NA12155, HG01522, NA18988, NA12341, NA20814, NA07346, HG01250, NA19373, NA19076, HG00272, NA18489, NA20589, NA19728, NA19448, NA19678, HG01167, NA20586, NA18982, NA18923, NA20317, NA18619, HG01492, HG00736, NA19062, NA11918, HG01354, NA19771, NA19457, HG00247, NA20513, NA19681, HG00185, NA20336, NA18964, HG00537, HG00311, NA20291, NA19130, NA19079, NA19720, HG01067, HG00120, NA20518, NA18874, NA20819, NA20812, NA18868, NA19719, NA19731, NA11994, NA18617, NA19385, NA19471, NA19317, NA18986, HG00182, NA19901, HG00637, HG00159, NA18557, HG01048, NA20342, NA19445, NA18908, NA18867, HG01550, NA19789, NA19921, NA19451, HG00739, HG00264, HG01136, HG00560, NA19082, HG01187, HG00328, HG00245, NA12342, NA19462, NA20809, NA18933, HG00577, HG01095, NA20810, NA20536, NA19717, NA20314, NA19236, HG00500, NA19788, NA12718, NA18910, HG01149, NA19064, HG01047, HG01094, HG00273, NA11919, NA19774, NA19000, NA19655, HG00373, NA11893, NA18856, HG00117, HG01101, HG00157, NA19257, NA19682, NA20828, NA19756, NA19469, NA19318, NA12546, NA19675, HG01204, NA20765, NA20526, NA20296, NA19685, HG00258, HG00124, HG00155, NA19440, HG00119, NA19390, HG00265, NA19834, NA19321, NA20815, NA18950, HG00734, NA19380, NA07051, NA19010, HG00098, NA19679, NA19439, NA19428, NA19311, HG00116, NA19083, NA20281, NA19085, HG01342, HG00269, NA19818, NA19759, NA19376, NA19785, NA19248, NA18631, NA19060, NA18987, HG01055, HG00174, HG00123, NA20510, NA19102, NA18873, HG00112, HG00131, NA11843, NA20758, NA19116, NA19780, NA19213, HG00377, HG00595, NA18984, NA07056, NA18989, NA18488, HG01082, NA19312, NA19463, NA19063, NA12154, NA19065, HG01112, NA18487, HG01437, NA19431, NA20509
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672564
Frequency
Sample Size1151
Observed Gain0
Observed Loss221
Observed Complex0
Frequencyn/a


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