A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751666



Internal ID20527526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46242982..46242982hg38UCSC Ensembl
chr3:46284473..46284473hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16259922
Samples
Known GenesCCR3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751666
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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