A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660753



Internal ID21609058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69821913..69821913hg38UCSC Ensembl
chr15:70114252..70114252hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383366
hg193366
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17093644
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660753
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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