A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3401959



Internal ID15248921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127033269..127033288hg38UCSC Ensembl
Innerchr11:127033265..127033292hg38UCSC Ensembl
Outerchr11:127033246..127033311hg38UCSC Ensembl
chr11:126903164..126903183hg19UCSC Ensembl
Innerchr11:126903160..126903187hg19UCSC Ensembl
Outerchr11:126903141..126903206hg19UCSC Ensembl
chr11:126408374..126408393hg18UCSC Ensembl
Innerchr11:126408397..126408370hg18UCSC Ensembl
Outerchr11:126408351..126408416hg18UCSC Ensembl
Cytoband11q24.2
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 Variantsessv9654603, essv9654592, essv9654614
SamplesNA12249, NA12043, NA12874
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3401959
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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