A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660081



Internal ID9926186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11369192..11369565hg38UCSC Ensembl
chr20:11349840..11350213hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38374
hg19374
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5603995, essv6009407, essv5647568, essv5567615, essv5456045, essv5707369, essv5632472, essv5775602, essv6557397, essv6248959, essv5880213, essv5733766, essv5934969, essv5954572, essv6552253, essv5902420, essv5648722, essv6255885, essv6591019, essv5668777, essv5842221, essv5977305, essv5648602, essv5613387, essv5594326, essv5728874, essv5984994, essv6007865
SamplesHG00096, HG01462, NA20332, HG01177, NA20586, NA18567, HG00270, HG00243, HG01134, NA20775, HG00154, HG00149, HG00145, NA19347, NA20521, HG00619, HG00284, HG00690, HG00258, NA20773, NA19440, NA19834, NA19072, NA18950, HG00123, HG00310, NA19726, NA20503
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660081
Frequency
Sample Size1151
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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