A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586459



Internal ID16373868
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 StatusM
Merged Variantsdgv7645n54
Supporting Variantsnssv941996, nssv942001, nssv942000, nssv941998, nssv941999, nssv942002, nssv941997
Samples
Known GenesTAF4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586459
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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