A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7759332



Internal ID14266208
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 StatusS
Merged Variantsesv3306590
Supporting Variants
SamplesNA18593
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7759332
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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