A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666841



Internal ID15403493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101813748..101822182hg38UCSC Ensembl
Innerchr9:104576030..104584464hg19UCSC Ensembl
Innerchr9:103615851..103624285hg18UCSC Ensembl
Innerchr9:101655585..101664019hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg388435
hg198435
hg188435
hg178435
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516211
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666841
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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