A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219174



Internal ID20786214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27178793..27180040hg38UCSC Ensembl
chr13:27752930..27754177hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg381248
hg191248
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579446
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219174
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