A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6253722



Internal ID9903429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55284466..55285324hg38UCSC Ensembl
chr14:55751184..55752042hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38859
hg19859
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657596
Supporting Variants
SamplesNA20798
Known GenesFBXO34
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6253722
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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