A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696744



Internal ID15433396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:26517802..26517999hg38UCSC Ensembl
Innerchr7:26557421..26557618hg19UCSC Ensembl
Innerchr7:26523946..26524143hg18UCSC Ensembl
Innerchr7:26330661..26330858hg17UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38198
hg19198
hg18198
hg17198
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519252
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696744
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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