A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17731841



Internal ID155507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:30936845..30977216hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3840372
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5527218
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17731841
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002811


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