A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1327n223



Internal ID22804295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122767083..122767382hg38UCSC Ensembl
chr11:122637791..122638090hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6579973, nsv6580684
Samples
Known GenesUBASH3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1327n223
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