A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5416563



Internal ID8393966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98235053..98236000hg38UCSC Ensembl
chr9:100997335..100998282hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38948
hg19948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2673798
Supporting Variants
SamplesNA19439
Known GenesTBC1D2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5416563
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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