A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668173



Internal ID9934278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:81663061..81706428hg38UCSC Ensembl
chr14:82129405..82172772hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3843368
hg1943368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5804438
SamplesNA19713
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668173
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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