A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6033418



Internal ID21942761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62362301..62362416hg38UCSC Ensembl
chr18:60029534..60029649hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626451
Samples
Known GenesTNFRSF11A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6033418
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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