A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199550



Internal ID20766590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5287174..5339457hg38UCSC Ensembl
chr19:5287185..5339468hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3852284
hg1952284
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521441
Supporting Variants
Samples
Known GenesPTPRS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199550
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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