A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14085896



Internal ID21289299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:128449171..128484422hg38UCSC Ensembl
Innerchr8:129461417..129496668hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3835252
hg1935252
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113610
Supporting Variants
Samplessample45
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14085896
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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