A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv939085



Internal ID16233041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:26294416..26328619hg38UCSC Ensembl
Innerchr20:26275052..26309255hg19UCSC Ensembl
Innerchr20:26223052..26257255hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3834204
hg1934204
hg1834204
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585817
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv939085
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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