A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv470884



Internal ID15386662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:22729735..22829773hg38UCSC Ensembl
Innerchr22:23072224..23171953hg19UCSC Ensembl
Innerchr22:21402224..21501953hg18UCSC Ensembl
Innerchr22:21396778..21496507hg16UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg38100039
hg1999730
hg1899730
hg1699730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv438338
Supporting Variants
SamplesNA18972
Known GenesMIR650
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)nssv470884
Frequency
Sample Size269
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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