A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv194e180



Internal ID22757604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61518913..61665737hg38UCSC Ensembl
chr9:44726751..44873575hg19UCSC Ensembl
chr9:44666747..44813571hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38146825
hg19146825
hg18146825
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv988098, esv994373
SamplesHuRef
Known Genes
MethodOligo aCGH
SNP array
AnalysisPooled samples.
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)dgv194e180
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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