A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv176n145



Internal ID22813192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102195357..102211837hg38UCSC Ensembl
chr10:103955114..103971594hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3816481
hg1916481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3115905, nsv3115524
Samplessample328, sample358, sample243
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv176n145
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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