A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588934



Internal ID16029657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33569653..33639048hg38UCSC Ensembl
Innerchr22:33965639..34035034hg19UCSC Ensembl
Innerchr22:32295639..32365034hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3869396
hg1969396
hg1869396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv954741
Samples
Known GenesLARGE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588934
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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