A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112734



Internal ID21296000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:95711047..95733549hg38UCSC Ensembl
Innerchr7:95340359..95362861hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3822503
hg1922503
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1119n145
Supporting Variantsnssv14084067
Samplessample15
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112734
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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