A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv942042



Internal ID16235998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62143364..62144236hg38UCSC Ensembl
Innerchr20:60718420..60719292hg19UCSC Ensembl
Innerchr20:60151815..60152687hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38873
hg19873
hg18873
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586477
Supporting Variants
Samples
Known GenesPSMA7, SS18L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv942042
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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