A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11952n54



Internal ID22779847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10383901..10436820hg38UCSC Ensembl
chr8:10241411..10294330hg19UCSC Ensembl
chr8:10278821..10331740hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3852920
hg1952920
hg1852920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv610265, nsv610266
Samples
Known GenesMSRA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11952n54
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