A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114476



Internal ID21297742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:46511725..46516672hg38UCSC Ensembl
Innerchr13:47085860..47090807hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg384948
hg194948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv290n145
Supporting Variantsnssv14094427
Samplessample64
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114476
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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