A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5110n223



Internal ID22808078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179690619..179691111hg38UCSC Ensembl
chr3:179408407..179408899hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38493
hg19493
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6567637, nsv6557451
Samples
Known GenesUSP13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5110n223
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