A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18267167



Internal ID20834207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:11122341..11124855hg38UCSC Ensembl
chr5:11122453..11124967hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg382515
hg192515
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569505
Supporting Variants
Samples
Known GenesCTNND2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18267167
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