A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14089301



Internal ID21267283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12943421..12949120hg38UCSC Ensembl
Innerchr4:12945045..12950744hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115668
Supporting Variants
Samplessample110
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14089301
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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