A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220407



Internal ID20787447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49044660..49045180hg38UCSC Ensembl
chr13:49618796..49619316hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587043
Supporting Variants
Samples
Known GenesFNDC3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220407
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