A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1822n54



Internal ID22769717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:54771612..55021565hg38UCSC Ensembl
chr11:51095992..51347668hg19UCSC Ensembl
chr11:50952568..51204244hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38249954
hg19251677
hg18251677
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554426, nsv554425
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1822n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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