A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614399



Internal ID21562704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145556777..145556777hg38UCSC Ensembl
chr3:145274564..145274564hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126828
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614399
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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