A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14099990



Internal ID21277449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59021221..59026023hg38UCSC Ensembl
Innerchr20:57596276..57601078hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg384803
hg194803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115460
Supporting Variants
Samplessample252
Known GenesTUBB1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14099990
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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