A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113332



Internal ID21296598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:79353926..79377568hg38UCSC Ensembl
Innerchr15:79646268..79669910hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3823643
hg1923643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096190
Samplessample161
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113332
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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