A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115787



Internal ID21299053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76942396..76951855hg38UCSC Ensembl
Innerchr15:77234737..77244196hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg389460
hg199460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096023
Samplessample60
Known GenesRCN2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115787
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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