A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766423



Internal ID20542283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69045532..69045532hg38UCSC Ensembl
chr15:69337872..69337872hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283175
Samples
Known GenesMIR548H4, NOX5
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766423
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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