A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv957064



Internal ID15904334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:39263768..39318699hg38UCSC Ensembl
Innerchr22:39659773..39714704hg19UCSC Ensembl
Innerchr22:37989719..38044650hg18UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3854932
hg1954932
hg1854932
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589033
Supporting Variants
Samples
Known GenesRNU86, RPL3, SNORD83A, SNORD83B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv957064
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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