A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699079



Internal ID15435731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:27183768..27241240hg38UCSC Ensembl
Innerchr13:27757905..27815377hg19UCSC Ensembl
Innerchr13:26655905..26713377hg18UCSC Ensembl
Innerchr13:26655905..26713377hg17UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3857473
hg1957473
hg1857473
hg1757473
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523333
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699079
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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