A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18253793



Internal ID20820833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40394636..40395326hg38UCSC Ensembl
chr22:40790640..40791330hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38691
hg19691
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6598643
Supporting Variants
Samples
Known GenesSGSM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18253793
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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