A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115655



Internal ID21298921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:75122147..75142755hg38UCSC Ensembl
Innerchr8:76034382..76054990hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3820609
hg1920609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087066
Samplessample109
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115655
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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