A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594999



Internal ID20968070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35691769..35692774hg38UCSC Ensembl
chr11:35713317..35714322hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381006
hg191006
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230514
Samples
Known GenesTRIM44
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594999
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