A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2141n54



Internal ID22770036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103256336..103408370hg38UCSC Ensembl
chr11:103127065..103279098hg19UCSC Ensembl
chr11:102632275..102784308hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38152035
hg19152034
hg18152034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556176, nsv556175
Samples
Known GenesDYNC2H1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2141n54
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