A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275901



Internal ID20842941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100919670..100925030hg38UCSC Ensembl
chr8:101931898..101937258hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg385361
hg195361
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569675
Supporting Variants
Samples
Known GenesYWHAZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275901
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