A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17729699



Internal ID153365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:48256860..48256966hg38UCSC Ensembl
chr22:48652672..48652778hg19UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5550403
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17729699
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.021698


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