A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3722n223



Internal ID22806690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54222701..54244500hg38UCSC Ensembl
chr19:54726573..54748341hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3821800
hg1921769
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6520285, nsv6524635
Samples
Known GenesLILRA6, LILRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3722n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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