A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16926129



Internal ID18158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:223685656..223715459hg38UCSC Ensembl
chr2:224550373..224580176hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg3829804
hg1929804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5435591
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16926129
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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