A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198022



Internal ID20765062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10369981..10370451hg38UCSC Ensembl
chr19:10480657..10481127hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516498
Supporting Variants
Samples
Known GenesTYK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198022
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00535


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