A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7327n223



Internal ID22810295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:43004104..43005743hg38UCSC Ensembl
chr8:42859247..42860886hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg381640
hg191640
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6560821, nsv6568391
Samples
Known GenesHOOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7327n223
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