A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657779



Internal ID21606084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89315541..89315541hg38UCSC Ensembl
chr15:89858772..89858772hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089985
SamplesNA20509
Known GenesFANCI
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657779
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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