A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704146



Internal ID127812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89855450..89868066hg38UCSC Ensembl
chr15:90398682..90411298hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3812617
hg1912617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5520072
Supporting Variants
Samples
Known GenesAP3S2, C15orf38-AP3S2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704146
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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