A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116009



Internal ID21299275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:20709618..20716493hg38UCSC Ensembl
Innerchr20:20690261..20697136hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg386876
hg196876
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14100744
Samplessample360
Known GenesRALGAPA2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116009
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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