A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110451



Internal ID21293717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:74647916..75350075hg38UCSC Ensembl
Innerchr3:74697067..75399226hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38702160
hg19702160
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14105981
Samplessample136
Known GenesMIR4444-1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110451
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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