A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115826



Internal ID21299092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:39821656..39826584hg38UCSC Ensembl
Innerchr20:38450298..38455226hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg384929
hg194929
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099777
Samplessample90
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115826
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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