A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116248



Internal ID21299514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:66125246..66128293hg38UCSC Ensembl
Innerchr7:65590233..65593280hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg383048
hg193048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1108n145
Supporting Variantsnssv14084387
Samplessample164
Known GenesCRCP
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116248
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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