A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv780n145



Internal ID22813796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:135001778..135024457hg38UCSC Ensembl
chr3:134720620..134743299hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg3822680
hg1922680
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3118259, nsv3112766
Samplessample54, sample295
Known GenesEPHB1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv780n145
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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