A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5811744



Internal ID8789147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57401519..57401924hg38UCSC Ensembl
chr14:57868237..57868642hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664347
Supporting Variants
SamplesNA12749
Known GenesNAA30
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5811744
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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