A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224295



Internal ID20791335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110179643..110180182hg38UCSC Ensembl
chr11:110050368..110050907hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38540
hg19540
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587563
Supporting Variants
Samples
Known GenesRDX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224295
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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