A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588932



Internal ID16029655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33470868..33536638hg38UCSC Ensembl
Innerchr22:33866854..33932624hg19UCSC Ensembl
Innerchr22:32196854..32262624hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3865771
hg1965771
hg1865771
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv954739
Samples
Known GenesLARGE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588932
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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