A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666528



Internal ID9585947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:89461363..89472612hg38UCSC Ensembl
Outerchr14:89461206..89472765hg38UCSC Ensembl
Innerchr14:89927707..89938956hg19UCSC Ensembl
Outerchr14:89927550..89939109hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3811560
hg1911560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5449594, essv6575079
SamplesNA20811, HG00236
Known GenesFOXN3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666528
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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