A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236739



Internal ID20803779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129520864..129522146hg38UCSC Ensembl
chr11:129390759..129392041hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg381283
hg191283
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575629
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236739
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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