A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092188



Internal ID21275826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:153242246..153245402hg38UCSC Ensembl
Innerchr4:154163398..154166554hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg383157
hg193157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110338
Supporting Variants
Samplessample228
Known GenesTRIM2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092188
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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