A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235564



Internal ID20802604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102437443..102438216hg38UCSC Ensembl
chr11:102308174..102308947hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg38774
hg19774
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580760
Supporting Variants
Samples
Known GenesTMEM123
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235564
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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