A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694253



Internal ID15430905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:28901735..28912107hg38UCSC Ensembl
Innerchr13:29475872..29486244hg19UCSC Ensembl
Innerchr13:28373872..28384244hg18UCSC Ensembl
Innerchr13:28373872..28384244hg17UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3810373
hg1910373
hg1810373
hg1710373
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518610
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694253
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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