A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232282



Internal ID20799322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111263677..111264197hg38UCSC Ensembl
chr11:111134402..111134922hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581429
Supporting Variants
Samples
Known GenesC11orf53
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232282
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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