A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657556



Internal ID21605861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87365010..87365010hg38UCSC Ensembl
chr16:87398616..87398616hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17095413
SamplesHG00732
Known GenesFBXO31
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657556
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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