A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116198



Internal ID21299464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:64535596..64538985hg38UCSC Ensembl
Innerchr8:65448153..65451542hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg383390
hg193390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087318
Samplessample300
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116198
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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