A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7837092



Internal ID14691736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79805833..79805834hg38UCSC Ensembl
Innerchr9:79805806..79805861hg38UCSC Ensembl
Outerchr9:79805805..79805862hg38UCSC Ensembl
chr9:82420748..82420749hg19UCSC Ensembl
Innerchr9:82420721..82420776hg19UCSC Ensembl
Outerchr9:82420720..82420777hg19UCSC Ensembl
chr9:81610568..81610569hg18UCSC Ensembl
Innerchr9:81610596..81610541hg18UCSC Ensembl
Outerchr9:81610540..81610597hg18UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38244
hg19244
hg18244
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3308499
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7837092
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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