A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645452



Internal ID21593757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69045556..69045556hg38UCSC Ensembl
chr15:69337896..69337896hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17079832
SamplesHG03125
Known GenesMIR548H4, NOX5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645452
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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