A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110517



Internal ID22019750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:16370596..18342386hg38UCSC Ensembl
chr16:16464453..18436243hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg381971791
hg191971791
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608730
Samples
Known GenesNPIPA7, NPIPA8, XYLT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110517
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