A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656832



Internal ID9576251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:25265625..25283531hg38UCSC Ensembl
Outerchr1:25265254..25283901hg38UCSC Ensembl
Innerchr1:25592116..25610022hg19UCSC Ensembl
Outerchr1:25591745..25610392hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3818648
hg1918648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6337337, essv5636855, essv6120121, essv6482795, essv6465670, essv5676232, essv5521057, essv6121943, essv6586123, essv5727396, essv6042063, essv5777756, essv5969740, essv6079016, essv5920003, essv6415878, essv6361179, essv6052654, essv6227566, essv6222588, essv6544420, essv6107254, essv6575867, essv5775494, essv5562400, essv5767672, essv5416946, essv5735325, essv5703613, essv6597030, essv6139482, essv5676997, essv5584210, essv6534784, essv6237647, essv6149601, essv6316228, essv6310525, essv6049915, essv6016439, essv5632957, essv6435338, essv5451781, essv5939418, essv5516471, essv5870973, essv6354502, essv5980877, essv6296342, essv5490325, essv5902927, essv5990190, essv5916446, essv6033167, essv5867377, essv5887710, essv6191013, essv5706326, essv5903420, essv6287382, essv5768634, essv5611603, essv5615723, essv5553671, essv6260838, essv6209943, essv5741443, essv6412577, essv5796702, essv5571873, essv5588552, essv6024054, essv6063162, essv5432168, essv5600122, essv6258093, essv6570589, essv6057359, essv6062519, essv5828384, essv6208047, essv5781714, essv5770421, essv6567765, essv6570509, essv6461358, essv6587900, essv5653207, essv6414935
SamplesHG00096, HG00189, HG00143, HG00231, HG00142, HG00249, HG00242, HG00100, HG00315, HG00151, HG00181, HG00179, HG00177, HG00150, HG00261, HG00337, HG00327, HG00138, HG00127, HG00272, HG00251, HG00122, HG00173, HG00330, HG00334, HG00185, HG00243, HG00158, HG00281, HG00277, HG00335, HG00148, HG00236, HG00156, HG00262, HG00182, HG00118, HG00338, HG00323, HG00253, HG00108, HG00313, HG00137, HG00133, HG00188, HG00268, HG00266, HG00176, HG00368, HG00344, HG00263, HG00275, HG00239, HG00324, HG00273, HG00321, HG00157, HG00140, HG01334, HG00152, HG00146, HG00126, HG00258, HG00124, HG00155, HG00254, HG00119, HG00336, HG00285, HG00265, HG00366, HG00353, HG00375, HG00357, HG00136, HG00278, HG00319, HG00116, HG00339, HG00329, HG00342, HG00174, HG00310, HG00131, HG00343, HG00377, HG00274, HG00252, HG00171
Known GenesRHD
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656832
Frequency
Sample Size1151
Observed Gain0
Observed Loss89
Observed Complex0
Frequencyn/a


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