A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3495n223



Internal ID22806463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32430151..32430812hg38UCSC Ensembl
chr19:32921057..32921718hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38662
hg19662
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6596860, nsv6596920
Samples
Known GenesDPY19L3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3495n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer