A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17718570



Internal ID142236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59438431..59438482hg38UCSC Ensembl
chr18:57105663..57105714hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5418448
Supporting Variants
Samples
Known GenesCCBE1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17718570
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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