A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv941992



Internal ID16235948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62064410..62066261hg38UCSC Ensembl
Innerchr20:60639466..60641317hg19UCSC Ensembl
Innerchr20:60072861..60074712hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381852
hg191852
hg181852
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586457
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)nssv941992
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