A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092371



Internal ID21278236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:18119397..18125441hg38UCSC Ensembl
Innerchr4:18121020..18127064hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg386045
hg196045
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114876
Supporting Variants
Samplessample266
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092371
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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