A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111676



Internal ID21294942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:73148438..73191594hg38UCSC Ensembl
Innerchr13:73722575..73765731hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3843157
hg1943157
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv302n145
Supporting Variantsnssv14095935
Samplessample345
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111676
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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