A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14100677



Internal ID21280379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59931976..59942258hg38UCSC Ensembl
Innerchr20:58507031..58517313hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3810283
hg1910283
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115511
Supporting Variants
Samplessample296
Known GenesFAM217B, PPP1R3D, SYCP2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14100677
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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