A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3303600



Internal ID15150548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:37415666..37415667hg38UCSC Ensembl
Innerchr15:37415636..37415697hg38UCSC Ensembl
Outerchr15:37415635..37415698hg38UCSC Ensembl
chr15:37707867..37707868hg19UCSC Ensembl
Innerchr15:37707837..37707898hg19UCSC Ensembl
Outerchr15:37707836..37707899hg19UCSC Ensembl
chr15:35495159..35495160hg18UCSC Ensembl
Innerchr15:35495190..35495129hg18UCSC Ensembl
Outerchr15:35495128..35495191hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38663
hg19663
hg18663
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7753858, essv7758054, essv7740810, essv7759691, essv7740664, essv7756916, essv7751346, essv7754389, essv7749123, essv7761870, essv7751316, essv7744358, essv7753107, essv7748740, essv7760518, essv7743014, essv7757547, essv7762967, essv7757070, essv7757758, essv7742864, essv7742561, essv7752446
SamplesNA12717, NA11830, NA11995, NA10851, NA12155, NA11992, NA12761, NA12156, NA11993, NA11831, NA12003, NA12878, NA18956, NA11919, NA11894, NA12249, NA12892, NA18564, NA07051, NA12763, NA12749, NA12154, NA12776
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3303600
Frequency
Sample Size185
Observed Gain23
Observed Loss0
Observed Complex0
Frequencyn/a


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