A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111367



Internal ID21294633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248574916..248630958hg38UCSC Ensembl
Innerchr1:248738217..248794259hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3856043
hg1956043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv133n145
Supporting Variantsnssv14106291
Samplessample63
Known GenesOR2T10, OR2T11
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111367
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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