A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520072



Internal ID296412
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 StatusM
Merged Variants
Supporting Variantsnssv17704146
Samples
Known GenesAP3S2, C15orf38-AP3S2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520072
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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