A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113546



Internal ID21296812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:41407114..41428995hg38UCSC Ensembl
Innerchr13:41981250..42003131hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3821882
hg1921882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14094364
Samplessample36
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113546
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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