A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091140



Internal ID21290889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:10491385..10517378hg38UCSC Ensembl
Innerchr11:10512932..10538925hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3825994
hg1925994
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112168
Supporting Variants
Samplessample66
Known GenesAMPD3, MIR4485, MTRNR2L8, RNF141
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091140
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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