A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17717460



Internal ID141126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38455267..38464893hg38UCSC Ensembl
chr18:36035231..36044857hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg389627
hg199627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5524869
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17717460
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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