A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254825



Internal ID20821865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:26017802..26017969hg38UCSC Ensembl
chr22:26413768..26413935hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596928
Supporting Variants
Samples
Known GenesMYO18B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254825
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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