A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14085763



Internal ID21291124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:92464722..92477944hg38UCSC Ensembl
Innerchr8:93476950..93490172hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3813223
hg1913223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112984
Supporting Variants
Samplessample7
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14085763
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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