A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615650



Internal ID7002539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156089668..156094157hg38UCSC Ensembl
Innerchr7:156089668..156094157hg38UCSC Ensembl
Outerchr7:156089290..156094430hg38UCSC Ensembl
chr7:155882362..155886851hg19UCSC Ensembl
Innerchr7:155882362..155886851hg19UCSC Ensembl
Outerchr7:155881984..155887124hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg384490
hg194490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13038307, essv13038298, essv13038311, essv13038319, essv13038296, essv13038318, essv13038315, essv13038308, essv13038314, essv13038309, essv13038301, essv13038304, essv13038312, essv13038300, essv13038310, essv13038299, essv13038306, essv13038303, essv13038316, essv13038297, essv13038317, essv13038302, essv13038295, essv13038305, essv13038313
SamplesHG01412, HG00142, HG01624, NA11933, HG01456, HG00097, HG01350, HG01277, HG01134, HG00148, HG01405, HG01440, HG01932, HG00338, NA20757, HG03585, HG01384, HG02142, HG01092, HG00146, HG01444, HG01272, HG01357, HG00274, HG01976
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615650
Frequency
Sample Size2504
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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