A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765673



Internal ID20541533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24512049..24512049hg38UCSC Ensembl
chr3:24553540..24553540hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292747
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765673
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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