A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752887



Internal ID20528747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128587091..128587091hg38UCSC Ensembl
chr3:128305934..128305934hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38465
hg19465
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266883
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752887
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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