A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657797



Internal ID9923902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:14389392..14389998hg38UCSC Ensembl
Outerchr4:14389021..14390368hg38UCSC Ensembl
Innerchr4:14391016..14391622hg19UCSC Ensembl
Outerchr4:14390645..14391992hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg381348
hg191348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6353584, essv5428998, essv5524306, essv5435831, essv6236986, essv5952165, essv5504938, essv6093409, essv5603164, essv5939140, essv5761639, essv5919141, essv6021972, essv5747676, essv5905298, essv6030162, essv5985703, essv6525133, essv6030826, essv6097130, essv5731376, essv6263845, essv6314269, essv5811501, essv5685215, essv5883518, essv6142358, essv6558652, essv5402455, essv6187861, essv6206733, essv6205042, essv5837309, essv6562731, essv6454847, essv5921799, essv5531201, essv5651414, essv5909366, essv5892269, essv5819014, essv5842093, essv6357463, essv6341836, essv6149867, essv6411535, essv5458977, essv6371778, essv6115410, essv6153158, essv5850815, essv6339605, essv6572361, essv5475510, essv5970747, essv5667335, essv6591484, essv6040474, essv6200147, essv5515207, essv6477173, essv5795047, essv6374636, essv6061566, essv5865934, essv5858505, essv6120808, essv6047039, essv6320117, essv5597131, essv6358265, essv6243130, essv6005298, essv6389136, essv6451276, essv6314296, essv6381277, essv5513746, essv5928385, essv5988136
SamplesHG00403, HG00650, HG00542, HG00442, HG00592, HG00536, HG00608, HG00671, HG00524, HG00699, HG00449, HG00654, HG00693, HG00663, HG00589, HG00501, HG00702, HG00689, HG00448, HG00634, HG00610, HG00537, HG00590, HG00512, HG00534, HG00422, HG00705, HG00427, HG00530, HG00419, HG00464, HG00543, HG00443, HG00596, HG00557, HG00428, HG00653, HG00701, HG00657, HG00475, HG00436, HG00556, HG00584, HG00533, HG00583, HG00500, HG00619, HG00708, HG00692, HG00651, HG00690, HG00404, HG00479, HG00684, HG00613, HG00525, HG00704, HG00463, HG00611, HG00476, HG00625, HG00565, HG00580, HG00473, HG00607, HG00662, HG00418, HG00620, HG00707, HG00672, HG00614, HG00513, HG00478, HG00421, HG00656, HG00698, HG00472, HG00628, HG00437, HG00581
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657797
Frequency
Sample Size1151
Observed Gain0
Observed Loss80
Observed Complex0
Frequencyn/a


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