A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv438056



Internal ID15387867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:56706147..56716663hg38UCSC Ensembl
Innerchr8:57618706..57629222hg19UCSC Ensembl
Innerchr8:57781260..57791776hg18UCSC Ensembl
Innerchr8:57668667..57679183hg16UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3810517
hg1910517
hg1810517
hg1610517
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv469981
SamplesNA18500
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)nsv438056
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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