A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv937960



Internal ID15885230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:11154259..11402679hg38UCSC Ensembl
Innerchr20:11134907..11383327hg19UCSC Ensembl
Innerchr20:11082907..11331327hg18UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38248421
hg19248421
hg18248421
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585415
Supporting Variants
Samples
Known GenesLOC339593
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv937960
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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