A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2656662

Internal ID9576081
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:79694317..79694399hg38UCSC Ensembl
Outerchr18:79694160..79694552hg38UCSC Ensembl
Innerchr18:77454317..77454399hg19UCSC Ensembl
Outerchr18:77454160..77454552hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5692443, essv6336995, essv6126164, essv5640588, essv6588492, essv6285425, essv6307918, essv6160467, essv5638216, essv6003957, essv5622995, essv5683784, essv6357758, essv6527595, essv5734835, essv5817329, essv6408394, essv5433200, essv5555965, essv5782234, essv5487995, essv6358693, essv6177697, essv6252977, essv6417932, essv5560595, essv5949827, essv6147289, essv6131103, essv5725466, essv6562767, essv6077243, essv6528088, essv5976379, essv5489873, essv6354924, essv6559190, essv5888186, essv6054894, essv6530473, essv5565576, essv5944265, essv5654535, essv6131678, essv5421345, essv5431876, essv6336297, essv6121153, essv5969419, essv5881420, essv5736317, essv6574880, essv6506319, essv5970364, essv6015570, essv5568194, essv6264709, essv6253441, essv5562146, essv6396363, essv6414835, essv5437161, essv6318479, essv6226236, essv5556955, essv5948143, essv5969063, essv5756650, essv6576985, essv5518678, essv6293739, essv6500663, essv5766158, essv6184835, essv6475422, essv5812352, essv6129506, essv5862632, essv5536922, essv5581525, essv5730073, essv5690228, essv5846344, essv6094658, essv6349969, essv5671042, essv5949220, essv5443303, essv6379327, essv5410468, essv6541438, essv5506460, essv6024788, essv6175800, essv6297050, essv6292823, essv6250951, essv5664957, essv6399523, essv5596415, essv6587605, essv5550205, essv5698985, essv6284285, essv6236254, essv6318342, essv6237760, essv6480091, essv5899710, essv6376959, essv5931088, essv6222358, essv6434717, essv5930965, essv6048094, essv6058473, essv5654041, essv6401683, essv6486751, essv5654766, essv5408567, essv6361412, essv6420815, essv6568765, essv5955718, essv5460344, essv5816136, essv6380105, essv6009307, essv6133424, essv6584671, essv6046428, essv5614809, essv6360462, essv6171502, essv6285704, essv6597828, essv5947147, essv6000859, essv6399204, essv5606723, essv6373614
SamplesHG01357, HG00613, HG01441, NA20281, HG00309, NA18964, NA12154, HG00537, HG00607, NA18595, NA20771, NA18951, HG00619, HG00418, HG01052, HG01519, HG01055, HG00705, HG00500, HG01173, HG01083, NA18501, NA20796, HG00310, NA18550, NA19072, HG00261, NA20802, NA20775, HG00463, HG00614, HG01051, HG01365, HG00428, HG00375, HG01174, HG00326, HG00139, NA19379, HG00701, HG00698, HG00334, HG00581, NA07051, HG01101, NA19257, HG00366, NA18505, NA18557, NA12287, NA20803, HG01171, HG00353, HG00479, NA20586, NA18632, HG00154, HG00242, HG01384, NA18624, HG00472, HG00421, NA18566, HG01378, NA18576, NA18622, NA18960, HG01048, HG01061, HG00231, HG00692, NA20801, HG00689, NA18636, NA19396, NA18592, HG00533, NA18609, HG00419, HG01360, NA12829, NA18637, NA20520, NA18916, HG00284, NA12830, NA18634, HG00237, HG00662, NA19360, HG00159, HG00233, HG00653, NA19374, NA20760, HG00325, NA18498, HG01073, HG00273, HG01069, HG00249, HG01080, HG01494, HG00329, NA19382, NA18606, HG00151, NA18987, NA18582, NA20756, HG00443, NA18599, NA19391, NA19009, HG00663, NA19116, HG00580, HG00448, NA18602, NA18577, HG00654, NA18548, HG00281, NA12546, HG00142, NA18571, NA19732, HG00422, NA18924, HG01108, NA11829, HG00275, HG00324, NA18532, NA20806, HG00684, NA18555, HG00271, NA19065, HG01067, HG00327, HG00361
Known GenesCTDP1
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)esv2656662
Sample Size1151
Observed Gain0
Observed Loss142
Observed Complex0

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