A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6218n223



Internal ID22809186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:65276232..67131267hg38UCSC Ensembl
chr6:65986125..67841160hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg381855036
hg191855036
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6558425, nsv6570019
Samples
Known GenesEYS, LOC441155, SLC25A51P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6218n223
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