A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232424



Internal ID20799464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:117990936..117991844hg38UCSC Ensembl
chr11:117861651..117862559hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38909
hg19909
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580399
Supporting Variants
Samples
Known GenesIL10RA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232424
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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