A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2201n54



Internal ID20135625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132056304..132060294hg38UCSC Ensembl
chr11:131926198..131930188hg19UCSC Ensembl
chr11:131431408..131435398hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383991
hg193991
hg183991
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556583, nsv556582
Samples
Known GenesNTM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2201n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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