A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074926



Internal ID20641966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45184993..45185709hg38UCSC Ensembl
chr22:45580874..45581590hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38717
hg19717
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549507
Supporting Variants
Samples
Known GenesNUP50
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074926
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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