A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113802



Internal ID21297068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:148073867..148076315hg38UCSC Ensembl
Innerchr6:148395003..148397451hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg382449
hg192449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1075n145
Supporting Variantsnssv14083846, nssv14083727, nssv14089191, nssv14086437
Samplessample145, sample390, sample68, sample278
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113802
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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