A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695760



Internal ID15432412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17965725..18017564hg38UCSC Ensembl
Innerchr9:17965723..18017562hg19UCSC Ensembl
Innerchr9:17955723..18007562hg18UCSC Ensembl
Innerchr9:17955723..18007562hg17UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3851840
hg1951840
hg1851840
hg1751840
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518330
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695760
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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