A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1816n54



Internal ID22769711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:50279041..50683696hg38UCSC Ensembl
chr11:50238212..50642867hg19UCSC Ensembl
chr11:50194788..50599443hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38404656
hg19404656
hg18404656
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554408, nsv554405
Samples
Known GenesLOC441601, LOC646813
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1816n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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