A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5994514



Internal ID21903857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9560064..9560214hg38UCSC Ensembl
chr3:9601748..9601898hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530772
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5994514
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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