A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17705413



Internal ID129079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86402819..86403581hg38UCSC Ensembl
chr15:86946050..86946812hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38763
hg19763
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5530462
Supporting Variants
Samples
Known GenesAGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17705413
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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