A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586614



Internal ID20959685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:86322624..86326177hg38UCSC Ensembl
chr13:86974879..86978432hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg383554
hg193554
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223036
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586614
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