A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110568



Internal ID21293834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72135808..72181337hg38UCSC Ensembl
Innerchr1:72601491..72647020hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3845530
hg1945530
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14089208, nssv14094283
Samplessample170, sample324
Known GenesNEGR1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110568
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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