A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668116



Internal ID9934221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3044654..3045523hg38UCSC Ensembl
chr11:3065884..3066753hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38870
hg19870
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5637223, essv5442353, essv6250810, essv6104879, essv5630778, essv5982071
SamplesHG00187, HG00369, HG00428, HG00276, HG00357, HG00345
Known GenesCARS
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668116
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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