A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230598



Internal ID20797638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110524327..110525243hg38UCSC Ensembl
chr12:110962132..110963048hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38917
hg19917
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578119
Supporting Variants
Samples
Known GenesRAD9B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230598
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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