A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1064n145



Internal ID22814080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117906260..117909852hg38UCSC Ensembl
chr6:118227423..118231015hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg383593
hg193593
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3116008, nsv3113156, nsv3110648
Samplessample289, sample224, sample14
Known GenesSLC35F1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1064n145
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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