A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109819



Internal ID22019052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73981972..73984366hg38UCSC Ensembl
chr11:73693017..73695411hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg382395
hg192395
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591488
Samples
Known GenesUCP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109819
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