A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761477



Internal ID20537337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145505077..145505077hg38UCSC Ensembl
chr3:145222864..145222864hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271299
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761477
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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