A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1080n145



Internal ID22814096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159725065..159730585hg38UCSC Ensembl
chr6:160146097..160151617hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg385521
hg195521
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3117594, nsv3111340
Samplessample81, sample300
Known GenesWTAP
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1080n145
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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