A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677093



Internal ID9943198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:92159167..92162203hg38UCSC Ensembl
Outerchr15:92159118..92162253hg38UCSC Ensembl
Innerchr15:92702397..92705433hg19UCSC Ensembl
Outerchr15:92702348..92705483hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg383136
hg193136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6573163
SamplesHG01342
Known GenesSLCO3A1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677093
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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