A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090582



Internal ID21271601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:120601255..120609593hg38UCSC Ensembl
Innerchr4:121522410..121530748hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg388339
hg198339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117570
Supporting Variants
Samplessample166
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090582
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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