A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114429



Internal ID21297695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:67339394..67340951hg38UCSC Ensembl
Innerchr8:68251629..68253186hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg381558
hg191558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14085347
Samplessample181
Known GenesARFGEF1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114429
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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