A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765322



Internal ID20541182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16309513..16309513hg38UCSC Ensembl
chr3:16351020..16351020hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38230
hg19230
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272576
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765322
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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