A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv954736



Internal ID15902006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33385806..33386721hg38UCSC Ensembl
Innerchr22:33781792..33782707hg19UCSC Ensembl
Innerchr22:32111792..32112707hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38916
hg19916
hg18916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv588929
Supporting Variants
Samples
Known GenesLARGE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv954736
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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