A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658404



Internal ID9924509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8023953..8025355hg38UCSC Ensembl
chr10:8065916..8067318hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381403
hg191403
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv117e199
Supporting Variantsessv5689036, essv5524099, essv6365762, essv6583485, essv5906889, essv5429438, essv5808867, essv6018718
SamplesNA18502, NA11829, NA19190, NA18579, NA18871, NA18853, NA19160, NA12776
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658404
Frequency
Sample Size1151
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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