A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11906n54



Internal ID20145330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:6934054..6936878hg38UCSC Ensembl
chr8:6791576..6794400hg19UCSC Ensembl
chr8:6778986..6781810hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg382825
hg192825
hg182825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv610013, nsv610014, nsv610015
Samples
Known GenesDEFA4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11906n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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