A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1704n54



Internal ID22769599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:24419419..24431228hg38UCSC Ensembl
chr11:24440965..24452774hg19UCSC Ensembl
chr11:24397541..24409350hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3811810
hg1911810
hg1811810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553796, nsv553795
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1704n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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