A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105399



Internal ID22014632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54047230..54047800hg38UCSC Ensembl
chr8:54959790..54960360hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38571
hg19571
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579224
Samples
Known GenesLYPLA1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105399
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