A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992324



Internal ID21901667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15987495..15987997hg38UCSC Ensembl
chr3:16029002..16029504hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38503
hg19503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17551955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992324
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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