A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116699



Internal ID21299965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:39782080..39790325hg38UCSC Ensembl
Innerchr15:40074281..40082526hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg388246
hg198246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096131
Samplessample131
Known GenesFSIP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116699
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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