A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv19e180



Internal ID20122958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3217492..3222899hg38UCSC Ensembl
chr11:3238722..3244129hg19UCSC Ensembl
chr11:3195298..3200705hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385408
hg195408
hg185408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv1006228, esv1006335
SamplesHuRef
Known GenesMRGPRG, MRGPRG-AS1
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)dgv19e180
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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