A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086280



Internal ID21278742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:110086985..110176941hg38UCSC Ensembl
Innerchr8:111099214..111189170hg19UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg3889957
hg1989957
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115453
Supporting Variants
Samplessample273
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086280
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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