A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227382



Internal ID20794422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:102059472..102059987hg38UCSC Ensembl
chr11:101930203..101930718hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38516
hg19516
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591145
Supporting Variants
Samples
Known GenesC11orf70
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227382
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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