A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520725



Internal ID15101332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:23157247..23343142hg38UCSC Ensembl
Innerchr13:23731386..23917281hg19UCSC Ensembl
Innerchr13:22629386..22815281hg18UCSC Ensembl
Innerchr13:22629386..22815281hg17UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg38185896
hg19185896
hg18185896
hg17185896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697577
Samples
Known GenesSACS, SGCG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520725
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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