A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1582n54



Internal ID22769477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4364953..4393849hg38UCSC Ensembl
chr11:4386183..4415079hg19UCSC Ensembl
chr11:4342759..4371655hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3828897
hg1928897
hg1828897
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553157, nsv553158, nsv553156
Samples
Known GenesOR52B4, TRIM21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1582n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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