A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756918



Internal ID20532778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86298252..86298252hg38UCSC Ensembl
chr15:86841483..86841483hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267348
Samples
Known GenesAGBL1, AGBL1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4756918
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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