A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233108



Internal ID20800148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118293855..118294558hg38UCSC Ensembl
chr12:118731660..118732363hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38704
hg19704
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591002
Supporting Variants
Samples
Known GenesTAOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233108
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00036


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