A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585733



Internal ID16373142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:24429559..24450589hg38UCSC Ensembl
Innerchr20:24410195..24431225hg19UCSC Ensembl
Innerchr20:24358195..24379225hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3821031
hg1921031
hg1821031
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152376
Samples1782681114_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585733
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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