A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3328n223



Internal ID22806296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24288483..24289690hg38UCSC Ensembl
chr18:21868447..21869654hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg381208
hg191208
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6594291, nsv6580042
Samples
Known GenesOSBPL1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3328n223
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