A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv113n145



Internal ID22813129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:219696378..219699951hg38UCSC Ensembl
chr1:219869720..219873293hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg383574
hg193574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3113223, nsv3115461, nsv3111117, nsv3111428
Samplessample206, sample299, sample79, sample68, sample117
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv113n145
Frequency
Sample Size467
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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