A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14082855



Internal ID21280338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:131947789..131953031hg38UCSC Ensembl
Innerchr6:132268929..132274171hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg385243
hg195243
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113104
Supporting Variants
Samplessample296
Known GenesCTGF
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14082855
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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