A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024777



Internal ID21934120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:67508233..67508311hg38UCSC Ensembl
chr18:65175470..65175548hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631790
Samples
Known GenesDSEL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024777
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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