A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662387



Internal ID9928492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:117173889..117176204hg38UCSC Ensembl
Outerchr11:117173732..117176357hg38UCSC Ensembl
Innerchr11:117044605..117046920hg19UCSC Ensembl
Outerchr11:117044448..117047073hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382626
hg192626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6253131
SamplesHG00428
Known GenesPAFAH1B2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662387
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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