A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv951874



Internal ID15899144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:20042355..20059164hg38UCSC Ensembl
Innerchr22:20029878..20046687hg19UCSC Ensembl
Innerchr22:18409878..18426687hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3816810
hg1916810
hg1816810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv588243
Supporting Variants
Samples
Known GenesTANGO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv951874
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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