A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1733n54



Internal ID22769628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29153190..29199747hg38UCSC Ensembl
chr11:29174737..29221294hg19UCSC Ensembl
chr11:29131313..29177870hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3846558
hg1946558
hg1846558
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553939, nsv553940
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1733n54
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