A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083914



Internal ID21287741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:40628131..40664617hg38UCSC Ensembl
Innerchr6:40595870..40632356hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3836487
hg1936487
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115914
Supporting Variants
Samplessample406
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083914
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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