A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220332



Internal ID20787372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104242098..104242413hg38UCSC Ensembl
chr12:104635876..104636191hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586040
Supporting Variants
Samples
Known GenesTXNRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220332
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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