A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1229n145



Internal ID22814245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:27570252..27575111hg38UCSC Ensembl
chr9:27570250..27575109hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg384860
hg194860
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3113420, nsv3111955, nsv3114226
Samplessample417, sample197, sample150
Known GenesC9orf72
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1229n145
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