A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12519n54



Internal ID22780414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:10647333..10686548hg38UCSC Ensembl
chr9:10647333..10686548hg19UCSC Ensembl
chr9:10637333..10676548hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3839216
hg1939216
hg1839216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613394, nsv613395
SamplesNINDS_209
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12519n54
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