A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658003



Internal ID9577422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31155108..31158939hg38UCSC Ensembl
Outerchr15:31155071..31158989hg38UCSC Ensembl
Innerchr15:31447311..31451142hg19UCSC Ensembl
Outerchr15:31447274..31451192hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg383919
hg193919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5504958
SamplesNA19788
Known GenesTRPM1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658003
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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