A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760725



Internal ID20536586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43178118..43178118hg38UCSC Ensembl
chr3:43219610..43219610hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16278085
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760725
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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