A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656564



Internal ID9922669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47194576..47197719hg38UCSC Ensembl
chr11:47216127..47219270hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg383144
hg193144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6244716, essv6258637, essv5414226, essv5830730
SamplesHG01079, NA19355, NA19777, NA19223
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656564
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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