A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092008



Internal ID21278700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18147511..18213735hg38UCSC Ensembl
Innerchr11:18169058..18235282hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3866225
hg1966225
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112386
Supporting Variants
Samplessample273
Known GenesLOC494141, MRGPRX4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092008
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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