A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108064



Internal ID21282805
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 StatusS
Merged Variantsnsv3117747
Supporting Variants
Samplessample331
Known GenesPTPRG
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108064
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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