A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3398000



Internal ID14898277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86484278..86484297hg38UCSC Ensembl
Innerchr11:86484274..86484301hg38UCSC Ensembl
Outerchr11:86484255..86484320hg38UCSC Ensembl
chr11:86195320..86195339hg19UCSC Ensembl
Innerchr11:86195316..86195343hg19UCSC Ensembl
Outerchr11:86195297..86195362hg19UCSC Ensembl
chr11:85872968..85872987hg18UCSC Ensembl
Innerchr11:85872991..85872964hg18UCSC Ensembl
Outerchr11:85872945..85873010hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9653325
SamplesNA12234
Known GenesME3
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3398000
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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