A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17609046



Internal ID21801093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89855550..89867425hg38UCSC Ensembl
chr15:90398782..90410657hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3811876
hg1911876
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6038364
Supporting Variants
Samples
Known GenesAP3S2, C15orf38-AP3S2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17609046
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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