A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667259



Internal ID9586678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110896948..110926081hg38UCSC Ensembl
chr9:113659228..113688361hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3829134
hg1929134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5753950
SamplesHG00533
Known GenesLPAR1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667259
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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