A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117747



Internal ID21301013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:61520537..61611680hg38UCSC Ensembl
Innerchr3:61506211..61597354hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3891144
hg1991144
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108064
Samplessample331
Known GenesPTPRG
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117747
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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