A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4733074



Internal ID20509001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:27280011..27282868hg38UCSC Ensembl
chr18:24859975..24862832hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg382858
hg192858
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294877
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4733074
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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