A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1011n145



Internal ID22814027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15466330..15473873hg38UCSC Ensembl
chr6:15466561..15474104hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg387544
hg197544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3112756, nsv3113503
Samplessample329, sample147
Known GenesJARID2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1011n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer