A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662986



Internal ID9929091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:69813710..69815784hg38UCSC Ensembl
Outerchr14:69813553..69815937hg38UCSC Ensembl
Innerchr14:70280427..70282501hg19UCSC Ensembl
Outerchr14:70280270..70282654hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg382385
hg192385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5512734
SamplesNA18870
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662986
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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