A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704496



Internal ID15441148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:32614394..32621380hg38UCSC Ensembl
Innerchr5:32614500..32621486hg19UCSC Ensembl
Innerchr5:32650257..32657243hg18UCSC Ensembl
Innerchr5:32650257..32657243hg17UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg386987
hg196987
hg186987
hg176987
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527979
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704496
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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