A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678964



Internal ID9598383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:12886188..12887371hg38UCSC Ensembl
Outerchr11:12886154..12887406hg38UCSC Ensembl
Innerchr11:12907735..12908918hg19UCSC Ensembl
Outerchr11:12907701..12908953hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg381253
hg191253
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv193e199
Supporting Variantsessv5889231
SamplesNA19082
Known GenesTEAD1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678964
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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