A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10266n54



Internal ID22778161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:348482..381918hg38UCSC Ensembl
chr6:348482..381918hg19UCSC Ensembl
chr6:293482..326918hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3833437
hg1933437
hg1833437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv600775, nsv600777, nsv600776, nsv600778
Samples
Known GenesDUSP22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10266n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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