A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv868n145



Internal ID22813884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26287955..26295480hg38UCSC Ensembl
chr4:26289577..26297102hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg387526
hg197526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3113845, nsv3113708
Samplessample369, sample120, sample32, sample35
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv868n145
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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