A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17621459



Internal ID21813506
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 StatusS
Merged Variantsnsv6110079
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17621459
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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