A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116516



Internal ID21299782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:81839997..81843220hg38UCSC Ensembl
Innerchr8:82752232..82755455hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg383224
hg193224
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086966
Samplessample81
Known GenesSNX16
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116516
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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