A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197700



Internal ID20764740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17411618..17416223hg38UCSC Ensembl
chr19:17522427..17527032hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg384606
hg194606
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6518426
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197700
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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