A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598890



Internal ID20971961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23014066..23014533hg38UCSC Ensembl
chr20:22994703..22995170hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38468
hg19468
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254294
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598890
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