A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4760402



Internal ID20536262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:27632897..27632897hg38UCSC Ensembl
chr3:27674388..27674388hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270139
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4760402
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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