A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667353



Internal ID9586772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1871900..1872182hg38UCSC Ensembl
chr11:1893130..1893412hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6302998, essv5641905, essv5557942, essv6159898, essv5770746, essv5430703, essv6436452
SamplesNA20281, NA20752, NA18960, NA20336, NA19728, NA19313, NA20289
Known GenesLSP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667353
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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