A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113503



Internal ID21296769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:15466330..15473873hg38UCSC Ensembl
Innerchr6:15466561..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 Variantsdgv1011n145
Supporting Variantsnssv14086449
Samplessample147
Known GenesJARID2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113503
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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