A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255583



Internal ID20822623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31546393..31548618hg38UCSC Ensembl
chr22:31942379..31944604hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg382226
hg192226
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600027
Supporting Variants
Samples
Known GenesSFI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255583
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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