A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588898



Internal ID16029621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33350638..33380444hg38UCSC Ensembl
Innerchr22:33746624..33776430hg19UCSC Ensembl
Innerchr22:32076624..32106430hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3829807
hg1929807
hg1829807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151740
SamplesHGDP00141
Known GenesLARGE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588898
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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