A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1537n54



Internal ID20134961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1279176..1397647hg38UCSC Ensembl
chr11:1300406..1418877hg19UCSC Ensembl
chr11:1256982..1375453hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38118472
hg19118472
hg18118472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552928, nsv552931
Samples
Known GenesBRSK2, TOLLIP, TOLLIP-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1537n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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