A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528493



Internal ID20901854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54219831..54239687hg38UCSC Ensembl
chr19:54723700..54743563hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3819857
hg1919864
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3718n223
Supporting Variantsnssv18200245
Samples
Known GenesLILRA6, LILRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528493
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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