A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276056



Internal ID20843096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:120730223..120730908hg38UCSC Ensembl
chr8:121742463..121743148hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38686
hg19686
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569890
Supporting Variants
Samples
Known GenesSNTB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276056
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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