A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933196



Internal ID22859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68127780..68127910hg38UCSC Ensembl
chr3:68176930..68177060hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5434529
Supporting Variants
Samples
Known GenesFAM19A1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933196
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.079145


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