A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv406n145



Internal ID22813422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51749793..51752829hg38UCSC Ensembl
chr15:52041990..52045026hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg383037
hg193037
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3113244, nsv3114663
Samplessample93, sample24
Known GenesLYSMD2, TMOD2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv406n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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