A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv438322



Internal ID15388132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:33896032..33897463hg38UCSC Ensembl
Innerchr21:35268336..35269767hg19UCSC Ensembl
Innerchr21:34190206..34191637hg18UCSC Ensembl
Innerchr21:34188732..34190163hg16UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg381432
hg191432
hg181432
hg161432
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv470801, nssv470802
SamplesNA10851, NA12763
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)nsv438322
Frequency
Sample Size269
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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