A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694799



Internal ID15431451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:27771815..27782185hg38UCSC Ensembl
Innerchr13:28345952..28356322hg19UCSC Ensembl
Innerchr13:27243952..27254322hg18UCSC Ensembl
Innerchr13:27243952..27254322hg17UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg3810371
hg1910371
hg1810371
hg1710371
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522030
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694799
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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