A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1655n54



Internal ID18993831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11840666..11854702hg38UCSC Ensembl
chr11:11862213..11876249hg19UCSC Ensembl
chr11:11818789..11832825hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3814037
hg1914037
hg1814037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553533, nsv553536, nsv553534, nsv553535
Samples
Known GenesUSP47
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1655n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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