A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv470875



Internal ID15386665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:22367510..22431601hg38UCSC Ensembl
Innerchr22:22721878..22785939hg19UCSC Ensembl
Innerchr22:21051878..21115939hg18UCSC Ensembl
Innerchr22:21046432..21110493hg16UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg3864092
hg1964062
hg1864062
hg1664062
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv438338
Supporting Variants
SamplesNA18972
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)nssv470875
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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