A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113376



Internal ID21296642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:200975..293446hg38UCSC Ensembl
Innerchr11:200975..293446hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3892472
hg1992472
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14091051
Samplessample143
Known GenesATHL1, BET1L, MIR6743, NLRP6, PSMD13, RIC8A, SIRT3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113376
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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