A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279223



Internal ID20846263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98084620..98086673hg38UCSC Ensembl
chr8:99096848..99098901hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg382054
hg192054
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567804
Supporting Variants
Samples
Known GenesC8orf47
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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