A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113808



Internal ID21297074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:50790636..50795182hg38UCSC Ensembl
Innerchr7:50858333..50862879hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg384547
hg194547
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1106n145
Supporting Variantsnssv14085675
Samplessample412
Known GenesGRB10
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113808
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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