A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073622



Internal ID20640662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33511906..33586124hg38UCSC Ensembl
chr22:33907892..33982110hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3874219
hg1974219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536934
Supporting Variants
Samples
Known GenesLARGE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073622
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