A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585334



Internal ID16372743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:5807139..5847729hg38UCSC Ensembl
Innerchr20:5787785..5828375hg19UCSC Ensembl
Innerchr20:5735785..5776375hg18UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3840591
hg1940591
hg1840591
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7449n54
Supporting Variantsnssv1152357
SamplesHGDP01281
Known GenesC20orf196
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585334
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