A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232513



Internal ID20799553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118733422..118735552hg38UCSC Ensembl
chr11:118604131..118606261hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382131
hg192131
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583270
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232513
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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