A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223322



Internal ID20790362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18513398..18514037hg38UCSC Ensembl
chr11:18534945..18535584hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38640
hg19640
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587485
Supporting Variants
Samples
Known GenesTSG101
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223322
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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