A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12366n54



Internal ID22780261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139765008..139810722hg38UCSC Ensembl
chr8:140777251..140822965hg19UCSC Ensembl
chr8:140846433..140892147hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3845715
hg1945715
hg1845715
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv612561, nsv612560
SamplesNINDS_111, HGDP00527
Known GenesTRAPPC9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12366n54
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