A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659584



Internal ID21607889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89325073..89325073hg38UCSC Ensembl
chr15:89868304..89868304hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38452
hg19452
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085308
SamplesNA24385
Known GenesPOLG
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659584
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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