A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11922n54



Internal ID20145346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:7486284..7497822hg38UCSC Ensembl
chr8:7343806..7355344hg19UCSC Ensembl
chr8:7331216..7342754hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3811539
hg1911539
hg1811539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv610081, nsv610082, nsv610080
Samples
Known GenesDEFB105A, DEFB105B, DEFB106A, DEFB106B, DEFB107A, DEFB107B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11922n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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