A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7746671



Internal ID14900187
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 StatusS
Merged Variantsesv3307394
Supporting Variants
SamplesNA19138
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7746671
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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