A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667454



Internal ID9933559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64342298..64363104hg38UCSC Ensembl
Outerchr9:64341927..64363474hg38UCSC Ensembl
Innerchr9:69354716..69375522hg19UCSC Ensembl
Outerchr9:69354345..69375892hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3821548
hg1921548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5436589, essv5876123, essv5489109, essv6410829, essv6563334, essv6397042, essv5745157, essv6515508, essv6577193, essv5516754, essv5409026, essv5468141, essv5515035, essv6366752, essv6280633, essv6325301, essv6303481, essv6417860, essv5405336, essv5642529, essv5962125, essv5526840, essv5455244, essv5887686, essv6390901, essv6086191, essv6084805, essv6560210, essv5422527, essv5787360, essv6000579, essv6296230, essv6463036, essv6575810, essv5987205, essv6534692, essv6488468, essv5785144, essv5475365, essv6447235, essv6068714, essv6427643
SamplesHG00403, HG00536, HG00608, HG00671, HG00699, HG00566, HG00449, HG00589, HG00501, HG00634, HG00590, HG00683, HG00422, HG00705, HG00530, HG00419, HG00464, HG00653, HG00577, HG00701, HG00657, HG00475, HG00556, HG00584, HG00500, HG00619, HG00651, HG00690, HG00479, HG00684, HG00611, HG00476, HG00473, HG00607, HG00418, HG00620, HG00614, HG00478, HG00656, HG00698, HG00595, HG00628
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667454
Frequency
Sample Size1151
Observed Gain0
Observed Loss42
Observed Complex0
Frequencyn/a


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