A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113483



Internal ID21296749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:102578251..102583900hg38UCSC Ensembl
Innerchr13:103230601..103236250hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg385650
hg195650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14094418
Samplessample60
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113483
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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