A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108746



Internal ID21286687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:39157534..39172411hg38UCSC Ensembl
Innerchr3:39199025..39213902hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3814878
hg1914878
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114549
Supporting Variants
Samplessample392
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108746
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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