A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276096



Internal ID20843136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:122341563..122342585hg38UCSC Ensembl
chr8:123353802..123354824hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg381023
hg191023
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561587
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276096
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00037


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