A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585663



Internal ID16373072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:17786928..17837496hg38UCSC Ensembl
Innerchr20:17767573..17818141hg19UCSC Ensembl
Innerchr20:17715573..17766141hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3850569
hg1950569
hg1850569
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv938592
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585663
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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