A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1679n223



Internal ID22804647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104256791..104257605hg38UCSC Ensembl
chr12:104650569..104651383hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38815
hg19815
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6588285, nsv6579538
Samples
Known GenesTXNRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1679n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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