A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218434



Internal ID20785474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118254806..118255904hg38UCSC Ensembl
chr12:118692611..118693709hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg381099
hg191099
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581090
Supporting Variants
Samples
Known GenesTAOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218434
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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