A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113253



Internal ID21296519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:148042932..148070346hg38UCSC Ensembl
Innerchr6:148364068..148391482hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg3827415
hg1927415
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14083758
Samplessample76
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113253
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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