A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593446



Internal ID20966517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102404853..102406615hg38UCSC Ensembl
chr11:102275584..102277346hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg381763
hg191763
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222806
Samples
Known GenesTMEM123
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593446
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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