A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14092579



Internal ID21280770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:248525274..248631888hg38UCSC Ensembl
Innerchr1:248688575..248795189hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38106615
hg19106615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111350
Supporting Variants
Samplessample302
Known GenesOR2T10, OR2T11, OR2T29, OR2T34
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14092579
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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