A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115716



Internal ID21298982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:77335537..77347062hg38UCSC Ensembl
Innerchr8:78247773..78259298hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3811526
hg1911526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086147
Samplessample232
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115716
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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