A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663084



Internal ID15399736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17638738..17662846hg38UCSC Ensembl
Innerchr5:17638847..17662955hg19UCSC Ensembl
Innerchr5:17671545..17695703hg18UCSC Ensembl
Innerchr5:17671545..17695703hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3824109
hg1924109
hg1824159
hg1724159
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)nssv663084
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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