A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672880



Internal ID9938985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:35391785..35429343hg38UCSC Ensembl
Outerchr15:35391748..35429393hg38UCSC Ensembl
Innerchr15:35683986..35721544hg19UCSC Ensembl
Outerchr15:35683949..35721594hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3837646
hg1937646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5797448
SamplesHG00262
Known GenesDPH6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672880
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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