A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17603473



Internal ID21795520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86693177..86901686hg38UCSC Ensembl
chr15:87236408..87444917hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38208510
hg19208510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6026113
Supporting Variants
Samples
Known GenesAGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17603473
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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