A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14106547



Internal ID21271499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:68580423..68591077hg38UCSC Ensembl
Innerchr3:68629574..68640228hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3810655
hg1910655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112565
Supporting Variants
Samplessample164
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14106547
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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