A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3440261



Internal ID15287214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:11650363..11650390hg38UCSC Ensembl
Innerchr11:11650367..11650386hg38UCSC Ensembl
Outerchr11:11650340..11650413hg38UCSC Ensembl
chr11:11671910..11671937hg19UCSC Ensembl
Innerchr11:11671914..11671933hg19UCSC Ensembl
Outerchr11:11671887..11671960hg19UCSC Ensembl
chr11:11628486..11628513hg18UCSC Ensembl
Innerchr11:11628509..11628490hg18UCSC Ensembl
Outerchr11:11628463..11628536hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38286
hg19286
hg18286
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8951526, essv8951525, essv8951523
SamplesNA18502, NA18912, NA18523
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3440261
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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