A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv935358



Internal ID16229314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1407668..1410039hg38UCSC Ensembl
Innerchr20:1388312..1390683hg19UCSC Ensembl
Innerchr20:1336312..1338683hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg382372
hg192372
hg182372
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585207
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)nssv935358
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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