A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111488



Internal ID21294754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:113388050..113392833hg38UCSC Ensembl
Innerchr1:113930672..113935455hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg384784
hg194784
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108411
Samplessample141
Known GenesMAGI3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111488
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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