A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv942039



Internal ID15889309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62140815..62144292hg38UCSC Ensembl
Innerchr20:60715871..60719348hg19UCSC Ensembl
Innerchr20:60149266..60152743hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg383478
hg193478
hg183478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586475
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)nssv942039
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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