A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236203



Internal ID20803243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110284646..110285395hg38UCSC Ensembl
chr11:110155371..110156120hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38750
hg19750
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592028
Supporting Variants
Samples
Known GenesRDX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236203
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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