A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695681



Internal ID15432333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:122779920..122794439hg38UCSC Ensembl
Innerchr9:125542199..125556718hg19UCSC Ensembl
Innerchr9:124582020..124596539hg18UCSC Ensembl
Innerchr9:122621753..122636272hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3814520
hg1914520
hg1814520
hg1714520
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518250
Supporting Variants
Samples
Known GenesOR5C1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695681
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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