A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112019



Internal ID21295285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:62798581..62802488hg38UCSC Ensembl
Innerchr18:60465814..60469721hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg383908
hg193908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv530n145
Supporting Variantsnssv14099582
Samplessample124
Known GenesPHLPP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112019
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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