A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489459



Internal ID22547378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:18048579..18049978hg38UCSC Ensembl
chr22:18531345..18532744hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878170
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489459
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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