A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111289



Internal ID22020522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:520078..713505hg38UCSC Ensembl
chr18:520078..713505hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38193428
hg19193428
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621431
Samples
Known GenesC18orf56, CETN1, CLUL1, ENOSF1, TYMS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111289
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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