A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1012n145



Internal ID22814028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15466494..15471549hg38UCSC Ensembl
chr6:15466725..15471780hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg385056
hg195056
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3117547, nsv3114746
Samplessample96, sample138
Known GenesJARID2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1012n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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