A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv59n21



Internal ID11600737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17379587..17413667hg38UCSC Ensembl
chr11:17401134..17435214hg19UCSC Ensembl
chr11:17357710..17391790hg18UCSC Ensembl
chr11:17357710..17391790hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3834081
hg1934081
hg1834081
hg1734081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv528959, nsv517772
Samples
Known GenesABCC8, KCNJ11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv59n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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