A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv51n21



Internal ID22766243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124995565..125004911hg38UCSC Ensembl
chr10:126684134..126693480hg19UCSC Ensembl
chr10:126674124..126683470hg18UCSC Ensembl
chr10:126674124..126683470hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg389347
hg199347
hg189347
hg179347
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv516502, nsv523644
Samples
Known GenesCTBP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv51n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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