A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5992044



Internal ID21901387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143046293..143085604hg38UCSC Ensembl
chr3:142765135..142804446hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3839312
hg1939312
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547817
Samples
Known GenesU2SURP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5992044
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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