A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3498n223



Internal ID22806466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35406215..35407482hg38UCSC Ensembl
chr19:35897117..35898384hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381268
hg191268
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6598688, nsv6599185
Samples
Known GenesLOC100128682
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3498n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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