A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659073



Internal ID9578492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89416349..89418352hg38UCSC Ensembl
Outerchr15:89416192..89418505hg38UCSC Ensembl
Innerchr15:89959580..89961583hg19UCSC Ensembl
Outerchr15:89959423..89961736hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg382314
hg192314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6315546, essv5903312
SamplesHG00692, NA18628
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659073
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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