A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697084



Internal ID15433736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113021309..113032379hg38UCSC Ensembl
Innerchr9:115783589..115794659hg19UCSC Ensembl
Innerchr9:114823410..114834480hg18UCSC Ensembl
Innerchr9:112863144..112874214hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3811071
hg1911071
hg1811071
hg1711071
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517282
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697084
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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