A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254901



Internal ID20821941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:18038126..18038611hg38UCSC Ensembl
chr22:18520892..18521377hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38486
hg19486
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596683
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254901
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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