A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117232



Internal ID21300498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11835793..11841830hg38UCSC Ensembl
Innerchr10:11877792..11883829hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg386038
hg196038
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089110
Samplessample103
Known GenesPROSER2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117232
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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