A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656662



Internal ID9576081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:79694317..79694399hg38UCSC Ensembl
Outerchr18:79694160..79694552hg38UCSC Ensembl
Innerchr18:77454317..77454399hg19UCSC Ensembl
Outerchr18:77454160..77454552hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38393
hg19393
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
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656662
Frequency
Sample Size1151
Observed Gain0
Observed Loss142
Observed Complex0
Frequencyn/a


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