A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074360



Internal ID20641400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42923498..42934932hg38UCSC Ensembl
chr22:43319504..43330938hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3811435
hg1911435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551234
Supporting Variants
Samples
Known GenesPACSIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074360
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