A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760677



Internal ID20536538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169780053..169780053hg38UCSC Ensembl
chr3:169497841..169497841hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg382460
hg192460
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276411
Samples
Known GenesMYNN
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760677
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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