A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115366



Internal ID21298632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:166648325..166649802hg38UCSC Ensembl
Innerchr1:166617562..166619039hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg381478
hg191478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108262
Samplessample8
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115366
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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