A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678186



Internal ID9944291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:39270429..39272092hg38UCSC Ensembl
Outerchr15:39270392..39272142hg38UCSC Ensembl
Innerchr15:39562630..39564293hg19UCSC Ensembl
Outerchr15:39562593..39564343hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg381751
hg191751
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5434525
SamplesNA12249
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678186
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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