A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589143



Internal ID16376552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:47322927..47391141hg38UCSC Ensembl
Innerchr22:47718677..47786891hg19UCSC Ensembl
Innerchr22:46097341..46165555hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3868215
hg1968215
hg1868215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8125n54
Supporting Variantsnssv957225
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589143
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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