A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586476



Internal ID16027199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62140816..62144394hg38UCSC Ensembl
Innerchr20:60715872..60719450hg19UCSC Ensembl
Innerchr20:60149267..60152845hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg383579
hg193579
hg183579
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv942040
Samples
Known GenesPSMA7, SS18L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586476
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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