A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv140n145



Internal ID22813156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11015525..11022220hg38UCSC Ensembl
chr10:11057488..11064183hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg386696
hg196696
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3113602, nsv3113237, nsv3117047, nsv3111085
Samplessample412, sample308, sample245, sample273
Known GenesCELF2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv140n145
Frequency
Sample Size467
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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