A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705536



Internal ID15442188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:111019706..111028751hg38UCSC Ensembl
Innerchr5:110355405..110364450hg19UCSC Ensembl
Innerchr5:110383304..110392349hg18UCSC Ensembl
Innerchr5:110383304..110392349hg17UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg389046
hg199046
hg189046
hg179046
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528857
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705536
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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