A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674280



Internal ID9593699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94810345..94966153hg38UCSC Ensembl
chr10:96570102..96725910hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38155809
hg19155809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6565531
SamplesNA19917
Known GenesCYP2C19, CYP2C9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674280
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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