A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660724



Internal ID9926829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:18964581..18964862hg38UCSC Ensembl
chr3:19006073..19006354hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6353013, essv6073326, essv5917969, essv5888151, essv6445077, essv6073984, essv6519647, essv6578104, essv5589319, essv5862861, essv6028444, essv5712301, essv5984704, essv5664720, essv5671738
SamplesHG01060, NA19703, NA18486, NA18504, NA18510, NA19446, HG01168, NA19383, NA19239, HG01073, NA19401, HG01108, NA19398, NA19102, NA19129
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660724
Frequency
Sample Size1151
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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