A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665704



Internal ID9931809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20032015..20032459hg38UCSC Ensembl
chr20:20012659..20013103hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38445
hg19445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6488171, essv5504428, essv6388495, essv5576646, essv5459456, essv6246983, essv5932673, essv5733074, essv6341980, essv5461265, essv5475479
SamplesNA18861, NA18870, NA19119, NA12287, NA19372, NA12828, NA19236, HG01102, NA19147, NA19439, NA19463
Known GenesNAA20
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665704
Frequency
Sample Size1151
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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