A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17715370



Internal ID139036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10220412..10225871hg38UCSC Ensembl
chr18:10220409..10225868hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg385460
hg195460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5516826
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17715370
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001718


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