A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589133



Internal ID20962204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8655033..8655807hg38UCSC Ensembl
chr11:8676580..8677354hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38775
hg19775
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231853
Samples
Known GenesTRIM66
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589133
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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