A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5990960



Internal ID21900303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:1091984..1965184hg38UCSC Ensembl
chr3:1133668..2006868hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38873201
hg19873201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519125
Samples
Known GenesCNTN6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5990960
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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