A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1071n145



Internal ID22814087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131947789..131953571hg38UCSC Ensembl
chr6:132268929..132274711hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg385783
hg195783
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3113104, nsv3117326
Samplessample404, sample300, sample378, sample397, sample296
Known GenesCTGF
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1071n145
Frequency
Sample Size467
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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