A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992221



Internal ID21901564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:187868482..187890222hg38UCSC Ensembl
chr3:187586270..187608010hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3821741
hg1921741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540933
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992221
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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