A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089082



Internal ID21292692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:90957334..90962162hg38UCSC Ensembl
Innerchr10:92717091..92721919hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg384829
hg194829
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111885
Supporting Variants
Samplessample90
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089082
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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