A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626404



Internal ID21574709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:444951..444951hg38UCSC Ensembl
chr8:394951..394951hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145638
SamplesHG00733
Known GenesFBXO25
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626404
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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