A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278078



Internal ID20845118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:43004353..43005743hg38UCSC Ensembl
chr8:42859496..42860886hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg381391
hg191391
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560821
Supporting Variants
Samples
Known GenesHOOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278078
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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