A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110750



Internal ID21294016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:63290854..63295062hg38UCSC Ensembl
Innerchr15:63583053..63587261hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg384209
hg194209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14096041
Samplessample72
Known GenesAPH1B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110750
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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