A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114861



Internal ID21298127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:24173561..24176022hg38UCSC Ensembl
Innerchr2:24396430..24398891hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg382462
hg192462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104618
Samplessample138
Known GenesFAM228A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114861
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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