A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254952



Internal ID20821992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37879088..37879494hg38UCSC Ensembl
chr22:38275095..38275501hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38407
hg19407
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598454
Supporting Variants
Samples
Known GenesEIF3L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254952
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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