A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277786



Internal ID20844826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33387510..33388346hg38UCSC Ensembl
chr8:33245028..33245864hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38837
hg19837
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557546
Supporting Variants
Samples
Known GenesFUT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277786
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