A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767221



Internal ID20543081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83888034..85841880hg38UCSC Ensembl
chr9:86502949..88456795hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg381953847
hg191953847
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16263216
Samples
Known GenesAGTPBP1, C9orf64, HNRNPK, KIF27, LOC389765, MIR7-1, NTRK2, RMI1, SLC28A3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767221
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