A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585862



Internal ID16373271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:30190681..30265572hg38UCSC Ensembl
Innerchr20:29425357..29500248hg19UCSC Ensembl
Innerchr20:28039018..28113909hg18UCSC Ensembl
Cytoband20q11.1
Allele length
AssemblyAllele length
hg3874892
hg1974892
hg1874892
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7547n54
Supporting Variantsnssv939181
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585862
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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