A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106913



Internal ID22016146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:310165..317944hg38UCSC Ensembl
chr11:310165..317944hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg387780
hg197780
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584465
Samples
Known GenesIFITM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106913
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