A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17725659



Internal ID149325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55344874..55350874hg38UCSC Ensembl
chr19:55856242..55862242hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6146362
Supporting Variants
Samples
Known GenesCOX6B2, SUV420H2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17725659
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.043937


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