A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090456



Internal ID21270214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:133861156..133879644hg38UCSC Ensembl
Innerchr4:134782311..134800799hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3818489
hg1918489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117409
Supporting Variants
Samplessample148
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090456
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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