A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv438321



Internal ID15041551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:32585524..32586037hg38UCSC Ensembl
Innerchr21:33957834..33958347hg19UCSC Ensembl
Innerchr21:32879705..32880218hg18UCSC Ensembl
Innerchr21:32878231..32878744hg16UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38514
hg19514
hg18514
hg16514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv470800
SamplesNA18945
Known GenesTCP10L
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)nsv438321
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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