A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589956



Internal ID18888237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:449912..517892hg38UCSC Ensembl
Innerchr20:430556..498536hg19UCSC Ensembl
Innerchr20:378556..446536hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3867981
hg1967981
hg1867981
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1063600
Supporting Variants
Samples
Known GenesCSNK2A1, TBC1D20
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3589956
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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