A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv82n199



Internal ID22802968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154589692..154614731hg38UCSC Ensembl
chrX:153817952..153842987hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3825040
hg1925036
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv4754521, nsv4754473
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)dgv82n199
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