A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3719n223



Internal ID22806687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54220401..54244400hg38UCSC Ensembl
chr19:54724271..54748241hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3824000
hg1923971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6528225, nsv6527806, nsv6533908
Samples
Known GenesLILRA6, LILRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3719n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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