A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv470079



Internal ID15039688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:21285390..21294922hg38UCSC Ensembl
Innerchr9:21285389..21294921hg19UCSC Ensembl
Innerchr9:21275389..21284921hg18UCSC Ensembl
Innerchr9:21275389..21284921hg16UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg389533
hg199533
hg189533
hg169533
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv438097
Supporting Variants
SamplesNA18914
Known Genes
MethodSNP array
AnalysisNull genotypes - for each genotype assay and population sample we defined the null genotype pattern of that assay as the binary vector (length 90) of null genotype calls across the 90 individuals.
PlatformNot reported
Comments
ReferenceMcCarroll_et_al_2006
Pubmed ID16468122
Accession Number(s)nssv470079
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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