A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200254



Internal ID20767294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54225201..54243000hg38UCSC Ensembl
chr19:54729073..54746849hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3817800
hg1917777
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524635
Supporting Variants
Samples
Known GenesLILRA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200254
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.20151


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