A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114464



Internal ID21297730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248547034..248632837hg38UCSC Ensembl
Innerchr1:248710335..248796138hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3885804
hg1985804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv132n145
Supporting Variantsnssv14094598, nssv14093282, nssv14090766
Samplessample242, sample312, sample308
Known GenesOR2T10, OR2T11, OR2T29, OR2T34
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114464
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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