A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580735



Internal ID20953806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:86797832..86907229hg38UCSC Ensembl
chr13:87450087..87559484hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38109398
hg19109398
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231332
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580735
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