A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992368



Internal ID21901711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170947168..170961116hg38UCSC Ensembl
chr3:170664957..170678905hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3813949
hg1913949
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552336
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992368
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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