A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5899623



Internal ID8877026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58509882..58512141hg38UCSC Ensembl
chr19:59021249..59023508hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg382260
hg192260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667957
Supporting Variants
SamplesNA19788
Known GenesSLC27A5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5899623
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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