A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991124



Internal ID21900467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:12878464..12881759hg38UCSC Ensembl
chr3:12919963..12923258hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg383296
hg193296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555940
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991124
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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