A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762277



Internal ID20538137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86410803..86410803hg38UCSC Ensembl
chr15:86954034..86954034hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16277845
Samples
Known GenesAGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762277
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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