A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3307669



Internal ID15154617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118003568..118003569hg38UCSC Ensembl
Innerchr11:118003531..118003606hg38UCSC Ensembl
Outerchr11:118003530..118003607hg38UCSC Ensembl
chr11:117874283..117874284hg19UCSC Ensembl
Innerchr11:117874246..117874321hg19UCSC Ensembl
Outerchr11:117874245..117874322hg19UCSC Ensembl
chr11:117379493..117379494hg18UCSC Ensembl
Innerchr11:117379531..117379456hg18UCSC Ensembl
Outerchr11:117379455..117379532hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38248
hg19248
hg18248
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7750653, essv7741369
SamplesNA18871, NA19257
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3307669
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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