A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3718n223



Internal ID22806686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54219831..54240000hg38UCSC Ensembl
chr19:54723700..54743876hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3820170
hg1920177
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6528493, nsv6522117, nsv6521759, nsv6526515
Samples
Known GenesLILRA6, LILRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3718n223
Frequency
Sample Size19652
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer