A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198112



Internal ID20765152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38872385..39331882hg38UCSC Ensembl
chr19:39363025..39822522hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38459498
hg19459498
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531882
Supporting Variants
Samples
Known GenesFBXO17, FBXO27, GMFG, IFNL1, IFNL2, IFNL3, IFNL4, LOC643669, LRFN1, MRPS12, NCCRP1, NFKBIB, PAK4, PAPL, RINL, SARS2, SIRT2, SYCN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198112
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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