A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3118028



Internal ID21301294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:73149918..73200987hg38UCSC Ensembl
Innerchr13:73724055..73775124hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3851070
hg1951070
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv302n145
Supporting Variantsnssv14095692
Samplessample192
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3118028
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer