A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275796



Internal ID20485014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:48367355..50080208hg38UCSC Ensembl
chr11:48388907..50039362hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg381712854
hg191650456
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754709
Supporting Variants
Samples
Known GenesFOLH1, LOC440040, OR4A47, OR4C12, OR4C13, TRIM49B, TRIM64C
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275796
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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