A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1007n145



Internal ID22814023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4773067..4779837hg38UCSC Ensembl
chr6:4773301..4780071hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg386771
hg196771
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3111282, nsv3114495, nsv3110650
Samplessample419, sample245, sample309
Known GenesCDYL
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1007n145
Frequency
Sample Size467
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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