A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254959



Internal ID20821999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38474946..38475879hg38UCSC Ensembl
chr22:38870951..38871884hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38934
hg19934
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599815
Supporting Variants
Samples
Known GenesKDELR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254959
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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