A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv78n199



Internal ID22802964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123977070..123993250hg38UCSC Ensembl
chr9:126739349..126755529hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3816181
hg1916181
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4758299, nsv4759907
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)dgv78n199
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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