A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv132n145



Internal ID22813148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:248525274..248632837hg38UCSC Ensembl
chr1:248688575..248796138hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38107564
hg19107564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3111350, nsv3117762, nsv3114464
Samplessample242, sample145, sample154, sample303, sample382, sample346, sample182, sample282, sample222, sample93, sample173, sample87, sample314, sample312, sample414, sample76, sample308, sample263, sample120, sample140, sample176, sample5, sample56, sample372, sample147, sample34, sample302, sample331, sample2, sample311, sample210, sample77, sample273, sample234, sample155, sample309, sample321, sample162, sample163, sample398
Known GenesOR2T10, OR2T11, OR2T29, OR2T34
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv132n145
Frequency
Sample Size467
Observed Gain0
Observed Loss40
Observed Complex0
Frequencyn/a


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