A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117819



Internal ID21301085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:78154477..78163722hg38UCSC Ensembl
Innerchr8:79066712..79075957hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg389246
hg199246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14085277
Samplessample162
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117819
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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