A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093222



Internal ID21284392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:88507083..88512044hg38UCSC Ensembl
Innerchr11:88240251..88245212hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg384962
hg194962
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112449
Supporting Variants
Samplessample360
Known GenesGRM5, GRM5-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093222
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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