A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668109



Internal ID9587528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:80484750..80485603hg38UCSC Ensembl
chr14:80951093..80951946hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38854
hg19854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5767103
SamplesNA18489
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668109
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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