A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv438107



Internal ID15041338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69491713..69494161hg38UCSC Ensembl
Innerchr9:72106629..72109077hg19UCSC Ensembl
Innerchr9:71296449..71298897hg18UCSC Ensembl
Innerchr9:67563748..67566196hg16UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg382449
hg192449
hg182449
hg162449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv470104
SamplesNA18953
Known GenesAPBA1
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)nsv438107
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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