A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228164



Internal ID20795204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121424775..121425853hg38UCSC Ensembl
chr11:121295484..121296562hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg381079
hg191079
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586709
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228164
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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