A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112718



Internal ID21295984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:89343653..89437794hg38UCSC Ensembl
Innerchr8:90355882..90450023hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3894142
hg1994142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14085864
Samplessample38
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112718
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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