A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1184n145



Internal ID22814200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:59732024..59739877hg38UCSC Ensembl
chr8:60644583..60652436hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg387854
hg197854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3114944, nsv3111972
Samplessample183, sample52
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1184n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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