A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660479



Internal ID21608784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88855709..88855709hg38UCSC Ensembl
chr15:89398940..89398940hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081349, nssv17091171
SamplesHG03125, NA24385
Known GenesACAN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660479
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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