A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026113



Internal ID21935456
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 StatusM
Merged Variants
Supporting Variantsnssv17603473
Samples
Known GenesAGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026113
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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