A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1504n54



Internal ID22769399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:173466..196533hg38UCSC Ensembl
chr11:173466..196533hg19UCSC Ensembl
chr11:163466..186533hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3823068
hg1923068
hg1823068
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv552756, nsv552758
Samples
Known GenesLOC653486, SCGB1C1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1504n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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