A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280852



Internal ID20490070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:18052985..18053145hg38UCSC Ensembl
chr22:18535751..18535911hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745680
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280852
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