A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114997



Internal ID21298263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:144481314..144612808hg38UCSC Ensembl
Innerchr3:144200156..144331650hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38131495
hg19131495
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14106580
Samplessample170
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114997
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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