A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv471248



Internal ID15386432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:35974941..36013897hg38UCSC Ensembl
Innerchr3:36016433..36055389hg19UCSC Ensembl
Innerchr3:35991437..36030393hg18UCSC Ensembl
Innerchr3:35977058..36016014hg16UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3838957
hg1938957
hg1838957
hg1638957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv438396
Supporting Variants
SamplesNA18944
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)nssv471248
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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