A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5955300



Internal ID9401746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:13136145..13146786hg38UCSC Ensembl
chr8:12993654..13004295hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3810642
hg1910642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669734
Supporting Variants
SamplesNA18606
Known GenesDLC1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5955300
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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