A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751923



Internal ID20527783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146635340..146635340hg38UCSC Ensembl
chr3:146353127..146353127hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258922
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751923
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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