A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112756



Internal ID21296022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:15467288..15473873hg38UCSC Ensembl
Innerchr6:15467519..15474104hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386586
hg196586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1011n145
Supporting Variantsnssv14082978
Samplessample329
Known GenesJARID2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112756
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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