A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586390



Internal ID16373799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:60828346..61128958hg38UCSC Ensembl
Innerchr20:59403402..59704014hg19UCSC Ensembl
Innerchr20:58836797..59137409hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38300613
hg19300613
hg18300613
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv941862
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586390
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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