A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114495



Internal ID21297761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4773067..4779129hg38UCSC Ensembl
Innerchr6:4773301..4779363hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg386063
hg196063
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1007n145
Supporting Variantsnssv14083967
Samplessample419
Known GenesCDYL
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114495
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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