A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752683



Internal ID20528543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145036246..145036246hg38UCSC Ensembl
chr3:144755088..144755088hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260552
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752683
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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