A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657986



Internal ID15394638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:102947839..102950144hg38UCSC Ensembl
Innerchr13:103600189..103602494hg19UCSC Ensembl
Innerchr13:102398190..102400495hg18UCSC Ensembl
Innerchr13:102398190..102400495hg17UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg382306
hg192306
hg182306
hg172306
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519731
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657986
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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