A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933111



Internal ID22797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62956000..63216000hg38UCSC Ensembl
chr3:62941675..63201676hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38260001
hg19260002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5436808
Supporting Variants
Samples
Known GenesLINC00698
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933111
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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