A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv952033



Internal ID16245989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:22438063..22485213hg38UCSC Ensembl
Innerchr22:22792400..22839559hg19UCSC Ensembl
Innerchr22:21122400..21169559hg18UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg3847151
hg1947160
hg1847160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv588460
Supporting Variants
Samples
Known GenesZNF280B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv952033
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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