A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112951



Internal ID21296217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:50995003..51014768hg38UCSC Ensembl
Innerchr15:51287200..51306965hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3819766
hg1919766
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098134
Samplessample391
Known GenesAP4E1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112951
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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