A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1564n54



Internal ID22769459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1752247..1785884hg38UCSC Ensembl
chr11:1773477..1807114hg19UCSC Ensembl
chr11:1730053..1763690hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3833638
hg1933638
hg1833638
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553049, nsv553048
Samples
Known GenesCTSD, MOB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1564n54
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