A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117756



Internal ID21301022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248576281..248631888hg38UCSC Ensembl
Innerchr1:248739582..248795189hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3855608
hg1955608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv133n145
Supporting Variantsnssv14091284, nssv14093095, nssv14083655, nssv14095960, nssv14089836, nssv14109160
Samplessample146, sample281, sample297, sample157, sample339, sample267
Known GenesOR2T10, OR2T11
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117756
Frequency
Sample Size467
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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