A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3717n223



Internal ID22806685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54217401..54278921hg38UCSC Ensembl
chr19:54721270..54782776hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3861521
hg1961507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6528784, nsv6534379, nsv6517398, nsv6522907
Samples
Known GenesLILRA6, LILRB2, LILRB3, LILRB5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3717n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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