A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16936805



Internal ID25256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97881506..97882061hg38UCSC Ensembl
chr3:97600350..97600905hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5448727
Supporting Variants
Samples
Known GenesCRYBG3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16936805
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer