A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12694n54



Internal ID22780589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:60994463..61002943hg38UCSC Ensembl
chr9:39964959..39973432hg19UCSC Ensembl
chr9:39954959..39963432hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg388481
hg198474
hg188474
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv614301, nsv614302
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12694n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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