A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659698



Internal ID9925803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:75873721..75883655hg38UCSC Ensembl
Outerchr15:75873684..75883705hg38UCSC Ensembl
Innerchr15:76166062..76175996hg19UCSC Ensembl
Outerchr15:76166025..76176046hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3810022
hg1910022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5558555
SamplesNA18986
Known GenesUBE2Q2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659698
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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