A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585759



Internal ID16373168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:25806460..25967691hg38UCSC Ensembl
Innerchr20:25787096..25948327hg19UCSC Ensembl
Innerchr20:25735096..25896327hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38161232
hg19161232
hg18161232
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7523n54
Supporting Variantsnssv938988
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585759
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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