A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14093456



Internal ID21280159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:45276549..45285657hg38UCSC Ensembl
Innerchr4:45278566..45287674hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg389109
hg199109
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112116
Supporting Variants
Samplessample293
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14093456
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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