A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646477



Internal ID21594782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40617347..40617347hg38UCSC Ensembl
chr13:41191484..41191484hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091024
SamplesHG01596
Known GenesFOXO1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646477
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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