A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12070n54



Internal ID19004246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25216199..25216845hg38UCSC Ensembl
chr8:25073715..25074361hg19UCSC Ensembl
chr8:25129632..25130278hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38647
hg19647
hg18647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv610836, nsv610838, nsv610839, nsv610835, nsv610837
Samples
Known GenesDOCK5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12070n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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