A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101617



Internal ID22010851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:24959877..25145983hg38UCSC Ensembl
chr11:24981423..25167529hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38186107
hg19186107
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584563
Samples
Known GenesLUZP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101617
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