A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1372e199



Internal ID20124674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111588610..111589796hg38UCSC Ensembl
chr9:114350890..114352076hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg381187
hg191187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2672152, esv2664348
SamplesNA18988
Known GenesPTGR1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1372e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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