A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14090182



Internal ID21270322
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 StatusS
Merged Variantsnsv3116474
Supporting Variants
Samplessample149
Known GenesPLCE1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14090182
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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