A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657299



Internal ID9576718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94690641..94698948hg38UCSC Ensembl
Outerchr10:94690484..94699101hg38UCSC Ensembl
Innerchr10:96450398..96458705hg19UCSC Ensembl
Outerchr10:96450241..96458858hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg388618
hg198618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6482050
SamplesHG00684
Known GenesCYP2C18
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657299
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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