A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702314



Internal ID125980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93852918..93858691hg38UCSC Ensembl
chr15:94396147..94401920hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg385774
hg195774
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520746
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702314
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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