A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2038n54



Internal ID20135462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82874314..82969697hg38UCSC Ensembl
chr11:82585356..82680739hg19UCSC Ensembl
chr11:82263004..82358387hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3895384
hg1995384
hg1895384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555603, nsv555601
Samples
Known GenesC11orf82, PRCP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2038n54
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