A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv388n145



Internal ID22813404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24847030..24849585hg38UCSC Ensembl
chr15:25092177..25094732hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg382556
hg192556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3115239, nsv3113997
Samplessample37, sample93, sample78, sample82, sample59
Known GenesSNRPN
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv388n145
Frequency
Sample Size467
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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