A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3307394



Internal ID15154342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87894602..87894603hg38UCSC Ensembl
Innerchr9:87894567..87894638hg38UCSC Ensembl
Outerchr9:87894566..87894639hg38UCSC Ensembl
chr9:90509517..90509518hg19UCSC Ensembl
Innerchr9:90509482..90509553hg19UCSC Ensembl
Outerchr9:90509481..90509554hg19UCSC Ensembl
chr9:89699337..89699338hg18UCSC Ensembl
Innerchr9:89699373..89699302hg18UCSC Ensembl
Outerchr9:89699301..89699374hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38116
hg19116
hg18116
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7762080, essv7761769, essv7759217, essv7746671, essv7745681, essv7760628, essv7743726, essv7757572, essv7756133, essv7756731
SamplesNA18508, NA18603, NA18870, NA18944, NA18582, NA19138, NA19238, NA18555, NA18576, NA12043
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3307394
Frequency
Sample Size185
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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