A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111479



Internal ID21294745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78793436..78814066hg38UCSC Ensembl
Innerchr6:79503153..79523783hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3820631
hg1920631
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1049n145
Supporting Variantsnssv14086385
Samplessample134
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111479
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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