A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611364



Internal ID21559669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51457991..51457991hg38UCSC Ensembl
chr3:51492007..51492007hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132256
SamplesNA18939
Known GenesVPRBP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611364
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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