A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255681



Internal ID20822721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47448371..47451402hg38UCSC Ensembl
chr22:47844120..47847151hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg383032
hg193032
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596387
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255681
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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