A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677755



Internal ID9943860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:127752712..127786060hg38UCSC Ensembl
Outerchr11:127752675..127786110hg38UCSC Ensembl
Innerchr11:127622607..127655955hg19UCSC Ensembl
Outerchr11:127622570..127656005hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3833436
hg1933436
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5622869
SamplesNA18576
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677755
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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