A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200245



Internal ID20767285
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 StatusS
Merged Variantsnsv6528493
Supporting Variants
Samples
Known GenesLILRA6, LILRB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200245
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.23767


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