A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615736



Internal ID21564041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:66766408..66766408hg38UCSC Ensembl
chr3:66816832..66816832hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120620
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615736
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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