A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255613



Internal ID20822653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40954051..40954840hg38UCSC Ensembl
chr22:41350055..41350844hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38790
hg19790
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596069
Supporting Variants
Samples
Known GenesRBX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255613
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