A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196219



Internal ID20763259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:22614267..22618763hg38UCSC Ensembl
chr18:20194230..20198726hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg384497
hg194497
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523299
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196219
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00043


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