A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991738



Internal ID21901081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128209262..128220182hg38UCSC Ensembl
chr3:127928105..127939025hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3810921
hg1910921
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555077
Samples
Known GenesEEFSEC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991738
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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