A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151741



Internal ID15507227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33710759..33830604hg38UCSC Ensembl
Innerchr22:34106745..34226592hg19UCSC Ensembl
Innerchr22:32436745..32556592hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38119846
hg19119848
hg18119848
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv588936
Supporting Variants
Samples1780854481_A
Known GenesLARGE, LARGE-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151741
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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