A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589957



Internal ID18888238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:449912..546851hg38UCSC Ensembl
Innerchr20:430556..527495hg19UCSC Ensembl
Innerchr20:378556..475495hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3896940
hg1996940
hg1896940
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055352
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)nssv3589957
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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