A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198919



Internal ID20765959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46735060..46735719hg38UCSC Ensembl
chr19:47238317..47238976hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38660
hg19660
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6519690
Supporting Variants
Samples
Known GenesSTRN4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198919
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00206


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