A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227152



Internal ID20794192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9682744..9683425hg38UCSC Ensembl
chr11:9704291..9704972hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38682
hg19682
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588067
Supporting Variants
Samples
Known GenesSWAP70
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227152
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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