A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661757



Internal ID9927862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:79672487..79679909hg38UCSC Ensembl
Outerchr15:79672450..79679959hg38UCSC Ensembl
Innerchr15:79964829..79972251hg19UCSC Ensembl
Outerchr15:79964792..79972301hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg387510
hg197510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5823065, essv5546682
SamplesNA19003, NA18941
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661757
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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