A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678304



Internal ID9944409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15188177..15190593hg38UCSC Ensembl
chr6:15188408..15190824hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg382417
hg192417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5408525, essv5962945, essv5885351, essv6439182, essv5559419, essv6122105, essv6100046, essv6033760, essv6081797, essv5791130, essv5433544, essv6251489, essv5485253, essv5827879, essv5735995, essv5832966, essv6135206, essv5890486, essv5604966, essv5718629, essv6045651, essv5941458, essv5435025
SamplesNA11830, NA20529, NA20802, HG00640, HG00337, HG00327, HG01070, NA20798, NA20524, HG00328, HG00732, HG00344, HG01073, HG00273, HG00373, HG00331, HG00258, HG00336, NA20804, HG00278, NA19428, HG00319, HG00174
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678304
Frequency
Sample Size1151
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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