A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3524n223



Internal ID22806492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40851312..41028609hg38UCSC Ensembl
chr19:41357217..41534514hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38177298
hg19177298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6522464, nsv6516669
Samples
Known GenesCYP2A7, CYP2B6, CYP2B7P, CYP2G1P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3524n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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