A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087805



Internal ID21277085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:13922491..13927390hg38UCSC Ensembl
Innerchr6:13922722..13927621hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg384900
hg194900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114440
Supporting Variants
Samplessample245
Known GenesRNF182
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087805
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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