A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083582



Internal ID21285135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:119032843..119056490hg38UCSC Ensembl
Innerchr6:119354008..119377655hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3823648
hg1923648
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115975
Supporting Variants
Samplessample37
Known GenesFAM184A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083582
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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