A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14082838



Internal ID21292546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:45093655..45133676hg38UCSC Ensembl
Innerchr6:45061392..45101413hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3840022
hg1940022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115577
Supporting Variants
Samplessample9
Known GenesSUPT3H
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14082838
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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