A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026466



Internal ID21935809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75554078..75555941hg38UCSC Ensembl
chr13:76128214..76130077hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg381864
hg191864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604028
Samples
Known GenesUCHL3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026466
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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