A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664348



Internal ID9583767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111588687..111589796hg38UCSC Ensembl
chr9:114350967..114352076hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg381110
hg191110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1372e199
Supporting Variantsessv5601532
SamplesNA18988
Known GenesPTGR1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664348
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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