A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672437



Internal ID9938542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:47598475..47601855hg38UCSC Ensembl
Outerchr11:47598438..47601905hg38UCSC Ensembl
Innerchr11:47620027..47623407hg19UCSC Ensembl
Outerchr11:47619990..47623457hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg383468
hg193468
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5425060
SamplesNA19235
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672437
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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