A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087313



Internal ID21280413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:102918937..102928125hg38UCSC Ensembl
Innerchr8:103931165..103940353hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg389189
hg199189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115903
Supporting Variants
Samplessample299
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087313
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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