A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5081n223



Internal ID22808049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169762301..169777100hg38UCSC Ensembl
chr3:169480089..169494888hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3814800
hg1914800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6373985, nsv6367562
Samples
Known GenesACTRT3, MYNN, TERC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5081n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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