A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17716803



Internal ID140469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26450490..26452572hg38UCSC Ensembl
chr18:24030454..24032536hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg382083
hg192083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5529951
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17716803
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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