A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112676



Internal ID21295942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:178721442..179029513hg38UCSC Ensembl
Innerchr4:179642596..179950667hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38308072
hg19308072
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14090703
Samplessample184
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112676
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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