A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117366



Internal ID21300632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:81872904..81896584hg38UCSC Ensembl
Innerchr8:82785139..82808819hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3823681
hg1923681
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087445
Samplessample335
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117366
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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