A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16263399



Internal ID20472617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:43515101..43515216hg38UCSC Ensembl
chr22:43910981..43911096hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743315
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16263399
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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