A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3452n223



Internal ID22806420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15711177..15904603hg38UCSC Ensembl
chr19:15821987..16015413hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38193427
hg19193427
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6597261, nsv6598034
Samples
Known GenesCYP4F2, CYP4F24P, OR10H1, OR10H2, OR10H3, OR10H5, UCA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3452n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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