A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3306590



Internal ID15153538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87331095..87331096hg38UCSC Ensembl
Innerchr9:87331064..87331127hg38UCSC Ensembl
Outerchr9:87331063..87331128hg38UCSC Ensembl
chr9:89946010..89946011hg19UCSC Ensembl
Innerchr9:89945979..89946042hg19UCSC Ensembl
Outerchr9:89945978..89946043hg19UCSC Ensembl
chr9:89135830..89135831hg18UCSC Ensembl
Innerchr9:89135862..89135799hg18UCSC Ensembl
Outerchr9:89135798..89135863hg18UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38309
hg19309
hg18309
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7744682, essv7743356, essv7754883, essv7751904, essv7741428, essv7745216, essv7752302, essv7759332, essv7748071, essv7742111, essv7747346, essv7762353, essv7751597, essv7746663, essv7754078, essv7747676, essv7762643, essv7749727, essv7748819, essv7743441, essv7755827, essv7748300, essv7742358, essv7761457, essv7752860, essv7757826, essv7751102, essv7756343, essv7755638, essv7746461, essv7745682
SamplesNA18592, NA18959, NA19190, NA07357, NA18550, NA18519, NA18960, NA18916, NA18571, NA19138, NA18605, NA18871, NA18573, NA18499, NA18912, NA18853, NA18555, NA18523, NA18858, NA18593, NA18542, NA19108, NA18943, NA19093, NA18609, NA19102, NA18505, NA07000, NA18562, NA18965, NA18577
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3306590
Frequency
Sample Size185
Observed Gain31
Observed Loss0
Observed Complex0
Frequencyn/a


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