A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089183



Internal ID21279007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:127653818..127768914hg38UCSC Ensembl
Innerchr6:127974963..128090059hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38115097
hg19115097
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114824
Supporting Variants
Samplessample276
Known GenesTHEMIS
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089183
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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