A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110479



Internal ID22019712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:21453524..22375265hg38UCSC Ensembl
chr5:21453633..22375374hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38921742
hg19921742
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547440
Samples
Known GenesCDH12, GUSBP1, PMCHL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110479
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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