A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689171



Internal ID15425823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:31959693..31961859hg38UCSC Ensembl
Innerchr13:32533830..32535996hg19UCSC Ensembl
Innerchr13:31431830..31433996hg18UCSC Ensembl
Innerchr13:31431830..31433996hg17UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg382167
hg192167
hg182167
hg172167
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517120
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689171
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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