A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv675419



Internal ID15412071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:3316877..3320018hg38UCSC Ensembl
Innerchr5:3316991..3320132hg19UCSC Ensembl
Innerchr5:3369991..3373132hg18UCSC Ensembl
Innerchr5:3369991..3373132hg17UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg383142
hg193142
hg183142
hg173142
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520787
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv675419
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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