A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117369



Internal ID21300635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:95711047..95730914hg38UCSC Ensembl
Innerchr7:95340359..95360226hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3819868
hg1919868
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1119n145
Supporting Variantsnssv14083350, nssv14085019
Samplessample90, sample404
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117369
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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