A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16930153



Internal ID20845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14415469..14421815hg38UCSC Ensembl
chr3:14456977..14463323hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg386347
hg196347
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5444209
Supporting Variants
Samples
Known GenesSLC6A6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16930153
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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