A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217237



Internal ID20784277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113550763..113553099hg38UCSC Ensembl
chr11:113421485..113423821hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg382337
hg192337
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583959
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217237
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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