A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676543



Internal ID9942648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:87510585..87517191hg38UCSC Ensembl
Outerchr15:87510214..87517561hg38UCSC Ensembl
Innerchr15:88053816..88060422hg19UCSC Ensembl
Outerchr15:88053445..88060792hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg387348
hg197348
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5976269, essv5443499, essv6357385, essv6210651, essv5722619, essv6139816, essv6191531, essv6257392, essv5761574, essv5526600, essv5742676, essv6105248, essv6577885, essv6229356, essv6555462, essv6270055, essv5679935, essv6353242, essv6362137, essv6169160, essv5586566, essv6596754, essv6425928, essv6285333, essv6316500, essv5957861, essv5663129, essv5791196, essv5492980, essv6063996, essv5608722, essv5446682, essv5823009, essv5429777, essv6109906, essv6395728, essv5804727, essv6449169, essv5904144, essv5974561, essv6529976, essv5667211, essv5724708
SamplesHG00315, HG00318, HG00337, HG00327, HG00271, HG00330, HG00346, HG00334, HG00281, HG00277, HG00335, HG00325, HG00309, HG00338, HG00326, HG00323, HG00313, HG00188, HG00268, HG00282, HG00328, HG00320, HG00344, HG00275, HG00324, HG00284, HG00273, HG00331, HG00321, HG00276, HG00336, HG00285, HG00353, HG00375, HG00278, HG00319, HG00339, HG00329, HG00342, HG00310, HG00280, HG00343, HG00345
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676543
Frequency
Sample Size1151
Observed Gain0
Observed Loss43
Observed Complex0
Frequencyn/a


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