A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111113



Internal ID21294379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:73392577..73412693hg38UCSC Ensembl
Innerchr13:73966714..73986830hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg3820117
hg1920117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14094352
Samplessample29
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111113
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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