A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12221n54



Internal ID22780116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:83616035..83648108hg38UCSC Ensembl
chr8:84528270..84560343hg19UCSC Ensembl
chr8:84690825..84722898hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3832074
hg1932074
hg1832074
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv611643, nsv611644
SamplesHGDP00141, HGDP00926
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12221n54
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