A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222246



Internal ID20789286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104338601..104338969hg38UCSC Ensembl
chr12:104732379..104732747hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38369
hg19369
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581854
Supporting Variants
Samples
Known GenesTXNRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222246
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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