A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654949



Internal ID15044915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:19889727..19890048hg38UCSC Ensembl
Innerchr13:20463867..20464188hg19UCSC Ensembl
Innerchr13:19361867..19362188hg18UCSC Ensembl
Innerchr13:19361867..19362188hg17UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38322
hg19322
hg18322
hg17322
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516945
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654949
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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