A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672347



Internal ID9591766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:132069208..132069878hg38UCSC Ensembl
Outerchr11:132069171..132069928hg38UCSC Ensembl
Innerchr11:131939102..131939772hg19UCSC Ensembl
Outerchr11:131939065..131939822hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38758
hg19758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6144676
SamplesHG00641
Known GenesNTM
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672347
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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