A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083162



Internal ID21285660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:131947789..131953571hg38UCSC Ensembl
Innerchr6:132268929..132274711hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg385783
hg195783
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117326
Supporting Variants
Samplessample378
Known GenesCTGF
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083162
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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