A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112018



Internal ID22021251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:47665415..49687026hg38UCSC Ensembl
chr18:45191786..47213396hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg382021612
hg192021611
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628689
Samples
Known GenesC18orf32, CTIF, DYM, LIPG, MIR1539, MIR4743, MIR4744, RPL17, RPL17-C18orf32, SMAD2, SMAD7, SNORD58A, SNORD58B, SNORD58C, ZBTB7C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112018
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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