A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5541795



Internal ID316351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45176477..45177323hg38UCSC Ensembl
chr22:45572358..45573204hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38847
hg19847
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17729463
Samples
Known GenesNUP50
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5541795
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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