A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16933022



Internal ID22738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58442428..58442479hg38UCSC Ensembl
chr3:58428155..58428206hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5395350
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16933022
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