A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615378



Internal ID21563683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27547868..27547868hg38UCSC Ensembl
chr3:27589359..27589359hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38379
hg19379
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124475
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615378
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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