A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657172



Internal ID15393824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17638738..17642407hg38UCSC Ensembl
Innerchr5:17638847..17642516hg19UCSC Ensembl
Innerchr5:17671545..17675214hg18UCSC Ensembl
Innerchr5:17671545..17675214hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg383670
hg193670
hg183670
hg173670
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516462
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657172
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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