A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658105



Internal ID9577524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:118410941..118412223hg38UCSC Ensembl
Innerchr11:118281656..118282938hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381283
hg191283
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6584321, essv5907849
SamplesNA19238, NA19240
Known GenesLOC100131626
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658105
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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