A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230480



Internal ID20797520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27677378..27678011hg38UCSC Ensembl
chr13:28251515..28252148hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38634
hg19634
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6590717
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230480
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