A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv954618



Internal ID15901888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33360030..33362894hg38UCSC Ensembl
Innerchr22:33756016..33758880hg19UCSC Ensembl
Innerchr22:32086016..32088880hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg382865
hg192865
hg182865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv588902
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)nssv954618
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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