A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991119



Internal ID21900462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128189755..128190058hg38UCSC Ensembl
chr3:127908598..127908901hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546808
Samples
Known GenesEEFSEC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991119
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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