A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657116



Internal ID15393768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:161639883..161642748hg38UCSC Ensembl
Innerchr5:161066889..161069754hg19UCSC Ensembl
Innerchr5:160999467..161002332hg18UCSC Ensembl
Innerchr5:160999467..161002332hg17UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg382866
hg192866
hg182866
hg172866
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515649
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657116
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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