A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033776



Internal ID21943119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:23469307..23469433hg38UCSC Ensembl
chr18:21049271..21049397hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624336
Samples
Known GenesRIOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033776
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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