A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1040n209



Internal ID22827115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40827499..41120720hg38UCSC Ensembl
chr19:41333404..41626625hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38293222
hg19293222
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5977639, nsv5969051
Samples
Known GenesCYP2A13, CYP2A6, CYP2A7, CYP2B6, CYP2B7P, CYP2F1, CYP2G1P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1040n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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