A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110079



Internal ID22019312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58417034..58417034hg38UCSC Ensembl
chr18:56084266..56084266hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17621459
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110079
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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