A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv83n21



Internal ID20131804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125200496..125218374hg38UCSC Ensembl
chr11:125070392..125088270hg19UCSC Ensembl
chr11:124575602..124593480hg18UCSC Ensembl
chr11:124575602..124593480hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3817879
hg1917879
hg1817879
hg1717879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv521936, nsv517656
Samples
Known GenesPKNOX2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv83n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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