A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12525n54



Internal ID22780420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11453474..11645495hg38UCSC Ensembl
chr9:11453474..11645495hg19UCSC Ensembl
chr9:11443474..11635495hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38192022
hg19192022
hg18192022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613429, nsv613430
SamplesHGDP00608
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12525n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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