A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4833n223



Internal ID22807801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32815401..32821900hg38UCSC Ensembl
chr3:32856893..32863392hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg386500
hg196500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6373663, nsv6373337
Samples
Known GenesTRIM71
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4833n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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