A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992181



Internal ID21901524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:181910308..181910477hg38UCSC Ensembl
chr3:181628096..181628265hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557358
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992181
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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