A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759752



Internal ID20535612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57998533..57998533hg38UCSC Ensembl
chr3:57984260..57984260hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16268064
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759752
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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