A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695558



Internal ID15432210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:133655586..133664817hg38UCSC Ensembl
Innerchr5:132991277..133000508hg19UCSC Ensembl
Innerchr5:133019176..133028407hg18UCSC Ensembl
Innerchr5:133019176..133028407hg17UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg389232
hg199232
hg189232
hg179232
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518138
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695558
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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