A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668518



Internal ID9934623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:25535894..25537046hg38UCSC Ensembl
chr11:25557440..25558592hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg381153
hg191153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv196e199
Supporting Variantsessv5681259, essv5888242, essv6292782, essv6484125
SamplesHG00650, NA18605, NA18546, HG00478
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668518
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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