A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207564



Internal ID20774604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45242180..45243753hg38UCSC Ensembl
chr22:45638061..45639634hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg381574
hg191574
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543415
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207564
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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