A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv69e180



Internal ID22757479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:50926732..50936025hg38UCSC Ensembl
chr17:49004093..49013386hg19UCSC Ensembl
chr17:46359092..46368385hg18UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg389294
hg199294
hg189294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv989743, esv1005053
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)dgv69e180
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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