A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv877n145



Internal ID22813893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:45276549..45285963hg38UCSC Ensembl
chr4:45278566..45287980hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg389415
hg199415
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3112964, nsv3112116
Samplessample293, sample339
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv877n145
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer