A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10655n54



Internal ID19002831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:49461993..49482628hg38UCSC Ensembl
chr6:49429706..49450341hg19UCSC Ensembl
chr6:49537665..49558300hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3820636
hg1920636
hg1820636
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv603089, nsv603090, nsv603085, nsv603083, nsv603084, nsv603088
Samples
Known GenesCENPQ, MUT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10655n54
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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