A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590379



Internal ID20963450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:49672787..49673588hg38UCSC Ensembl
chr13:50246923..50247724hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219370
Samples
Known GenesEBPL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590379
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer