A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117226



Internal ID21300492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:42392294..42393582hg38UCSC Ensembl
Innerchr8:42249812..42251100hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg381289
hg191289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087184
Samplessample136
Known GenesVDAC3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117226
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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