A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111496



Internal ID21294762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:123396378..123401135hg38UCSC Ensembl
Innerchr4:124317533..124322290hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg384758
hg194758
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv922n145
Supporting Variantsnssv14094942
Samplessample397
Known GenesSPRY1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111496
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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