A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5016n223



Internal ID22807984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129339101..129365600hg38UCSC Ensembl
chr3:129057944..129084443hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3826500
hg1926500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6368401, nsv6368912
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5016n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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