A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18198903



Internal ID20765943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46111927..46126100hg38UCSC Ensembl
chr19:46615185..46629357hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3814174
hg1914173
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533500
Supporting Variants
Samples
Known GenesIGFL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18198903
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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