A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116474



Internal ID21299740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:93993226..93995521hg38UCSC Ensembl
Innerchr10:95752983..95755278hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg382296
hg192296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14090182
Samplessample149
Known GenesPLCE1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116474
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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