A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv437876



Internal ID15388226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:104899129..104912759hg38UCSC Ensembl
Innerchr3:104617973..104631603hg19UCSC Ensembl
Innerchr3:106100663..106114293hg18UCSC Ensembl
Innerchr3:105938874..105952504hg16UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3813631
hg1913631
hg1813631
hg1613631
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv471352
SamplesNA18966
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)nsv437876
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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