A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18249901



Internal ID20816942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12116680..12117083hg38UCSC Ensembl
chr1:12176737..12177140hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541927
Supporting Variants
Samples
Known GenesTNFRSF8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18249901
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