A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1976n54



Internal ID20135400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67141279..67149366hg38UCSC Ensembl
chr11:66908750..66916837hg19UCSC Ensembl
chr11:66665326..66673413hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg388088
hg198088
hg188088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555247, nsv555248, nsv555250, nsv555249, nsv555251
Samples
Known GenesKDM2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1976n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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