A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666297



Internal ID9932402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:89734531..89737382hg38UCSC Ensembl
Outerchr14:89734374..89737535hg38UCSC Ensembl
Innerchr14:90200875..90203726hg19UCSC Ensembl
Outerchr14:90200718..90203879hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg383162
hg193162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5754272
SamplesHG00436
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666297
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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