A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667267



Internal ID9933372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:64082917..64087723hg38UCSC Ensembl
Outerchr15:64082546..64088093hg38UCSC Ensembl
Innerchr15:64375116..64379922hg19UCSC Ensembl
Outerchr15:64374745..64380292hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg385548
hg195548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6542171, essv5467572, essv6523139, essv6330931, essv6153031, essv5677956, essv6074263, essv5963373, essv6182820, essv5696021, essv6445342, essv5434894, essv5465605, essv5930961, essv6186747, essv6574375, essv6415419, essv6379207, essv5607362, essv5868484, essv5869508, essv6399156, essv5536496, essv6041460, essv5751125, essv5575215, essv6529644, essv5730386, essv6310934, essv5683234, essv6584722, essv5964490, essv6591491, essv6477464, essv5767515, essv5958626, essv5922665, essv6159111, essv5624495, essv5904513, essv6147807, essv5537332, essv5876102, essv6348022, essv6205912, essv5470606, essv5610162, essv6060090, essv5926973, essv6194332, essv6340569, essv6571266, essv6511143
SamplesHG00626, HG00403, HG00650, HG00542, HG00442, HG00536, HG00608, HG00524, HG00699, HG00449, HG00654, HG00663, HG00589, HG00501, HG00702, HG00689, HG00448, HG00537, HG00512, HG00534, HG00705, HG00530, HG00464, HG00543, HG00629, HG00443, HG00557, HG00428, HG00701, HG00475, HG00556, HG00584, HG00533, HG00500, HG00619, HG00708, HG00692, HG00651, HG00690, HG00684, HG00525, HG00463, HG00476, HG00580, HG00607, HG00418, HG00620, HG00707, HG00614, HG00513, HG00478, HG00698, HG00581
Known GenesFAM96A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667267
Frequency
Sample Size1151
Observed Gain0
Observed Loss53
Observed Complex0
Frequencyn/a


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