A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv942020



Internal ID16235976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62064568..62066551hg38UCSC Ensembl
Innerchr20:60639624..60641607hg19UCSC Ensembl
Innerchr20:60073019..60075002hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381984
hg191984
hg181984
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586463
Supporting Variants
Samples
Known GenesTAF4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv942020
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer