A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5958503



Internal ID8935906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27826528..27826814hg38UCSC Ensembl
chr8:27684045..27684331hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38287
hg19287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2668206
Supporting Variants
SamplesNA18565
Known GenesPBK
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5958503
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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