A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991265



Internal ID21900608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128558380..128558667hg38UCSC Ensembl
chr3:128277223..128277510hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547466
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991265
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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