A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14103091



Internal ID21281174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:40042966..40046479hg38UCSC Ensembl
Innerchr22:40438970..40442483hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg383514
hg193514
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110623
Supporting Variants
Samplessample309
Known GenesTNRC6B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14103091
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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