A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589969



Internal ID20963040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110280982..110281543hg38UCSC Ensembl
chr11:110151707..110152268hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38562
hg19562
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220550
Samples
Known GenesRDX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589969
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