A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671991



Internal ID9938096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98044322..98044573hg38UCSC Ensembl
chr10:99804079..99804330hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5531430, essv5638659, essv6530032, essv5559356, essv5722323, essv5468653, essv6566888, essv6405999, essv5984680, essv5449264, essv6108298
SamplesNA18861, NA19359, NA19819, HG01083, NA19904, NA18868, NA18853, NA18909, NA19434, NA19116, NA19129
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671991
Frequency
Sample Size1151
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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