A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116584



Internal ID21299850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:124215812..124225184hg38UCSC Ensembl
Innerchr11:124086519..124095889hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg389373
hg199371
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv228n145
Supporting Variantsnssv14091938, nssv14091014, nssv14091996, nssv14090911, nssv14091951, nssv14093089, nssv14089989
Samplessample90, sample303, sample9, sample128, sample244, sample246, sample268
Known GenesOR8G2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116584
Frequency
Sample Size467
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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