A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761528



Internal ID20537388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169769185..169769185hg38UCSC Ensembl
chr3:169486973..169486973hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267528
Samples
Known GenesACTRT3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761528
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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