A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv468232



Internal ID15387475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:21371423..21374194hg38UCSC Ensembl
Innerchr4:21373046..21375817hg19UCSC Ensembl
Innerchr4:20982144..20984915hg18UCSC Ensembl
Innerchr4:21123929..21126700hg16UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg382772
hg192772
hg182772
hg162772
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv437914
Supporting Variants
SamplesNA19201
Known GenesKCNIP4
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)nssv468232
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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