A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696198



Internal ID15432850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:4619872..4629402hg38UCSC Ensembl
Innerchr17:4523167..4532697hg19UCSC Ensembl
Innerchr17:4469916..4479446hg18UCSC Ensembl
Innerchr17:4469916..4479446hg17UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg389531
hg199531
hg189531
hg179531
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518749
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696198
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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