A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16963363



Internal ID42901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32225237..32225290hg38UCSC Ensembl
chr5:32225343..32225396hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5453991
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16963363
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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