A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2656832

Internal ID9576251
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25265625..25283531hg38UCSC Ensembl
Outerchr1:25265254..25283901hg38UCSC Ensembl
Innerchr1:25592116..25610022hg19UCSC Ensembl
Outerchr1:25591745..25610392hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6465670, essv6079016, essv6570509, essv5990190, essv5735325, essv5775494, essv6415878, essv5902927, essv6260838, essv5867377, essv6296342, essv5777756, essv5870973, essv5615723, essv6149601, essv5600122, essv5781714, essv6567765, essv6227566, essv6016439, essv6052654, essv6575867, essv6107254, essv5706326, essv5521057, essv5903420, essv5432168, essv5703613, essv5767672, essv6062519, essv5828384, essv6063162, essv6139482, essv6534784, essv5451781, essv6544420, essv6316228, essv6482795, essv5796702, essv6597030, essv5611603, essv5916446, essv5770421, essv5768634, essv5887710, essv6587900, essv5516471, essv5562400, essv5588552, essv5416946, essv6354502, essv6209943, essv5980877, essv5939418, essv5636855, essv6414935, essv6057359, essv5969740, essv5676997, essv6412577, essv5553671, essv6121943, essv6258093, essv5676232, essv6237647, essv6570589, essv5584210, essv6337337, essv6049915, essv6435338, essv6287382, essv5741443, essv6024054, essv6042063, essv6361179, essv6120121, essv6310525, essv6222588, essv5490325, essv5727396, essv5653207, essv5632957, essv6586123, essv6208047, essv5920003, essv5571873, essv6461358, essv6191013, essv6033167
SamplesHG00323, HG00157, HG00313, HG00152, HG00252, HG00182, HG00344, HG00100, HG00127, HG00171, HG00274, HG00131, HG00155, HG00310, HG00261, HG00189, HG00375, HG00368, HG00173, HG00148, HG00122, HG00334, HG00335, HG00366, HG00177, HG00146, HG00319, HG00253, HG00156, HG00188, HG00353, HG00342, HG00266, HG00321, HG00339, HG00158, HG00242, HG00179, HG00337, HG00140, HG00096, HG00231, HG00315, HG00330, HG00338, HG00150, HG00258, HG00174, HG00243, HG00254, HG00357, HG00343, HG00133, HG00124, HG00108, HG00268, HG00185, HG00263, HG00176, HG00239, HG00265, HG00273, HG00249, HG00116, HG00277, HG00329, HG00377, HG00236, HG00151, HG00181, HG01334, HG00138, HG00262, HG00118, HG00281, HG00285, HG00142, HG00251, HG00119, HG00275, HG00324, HG00137, HG00143, HG00336, HG00272, HG00278, HG00136, HG00126, HG00327
Known GenesRHD
AnalysisNo reference, merging analysis
CommentsHigh quality site
Pubmed ID23128226
Accession Number(s)esv2656832
Sample Size1151
Observed Gain0
Observed Loss89
Observed Complex0

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