A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113475



Internal ID21296741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:93992188..93995775hg38UCSC Ensembl
Innerchr10:95751945..95755532hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg383588
hg193588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088583
Samplessample208
Known GenesPLCE1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113475
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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