A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv942002



Internal ID16235958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62064410..62066551hg38UCSC Ensembl
Innerchr20:60639466..60641607hg19UCSC Ensembl
Innerchr20:60072861..60075002hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg382142
hg192142
hg182142
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586459
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)nssv942002
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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