A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1705n223



Internal ID22804673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118254806..118255913hg38UCSC Ensembl
chr12:118692611..118693718hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg381108
hg191108
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6578453, nsv6581090
Samples
Known GenesTAOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1705n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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