A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7737240



Internal ID13901859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:118846554..118854258hg38UCSC Ensembl
Outerchr9:118846354..118854458hg38UCSC Ensembl
Innerchr9:121608832..121616536hg19UCSC Ensembl
Outerchr9:121608632..121616736hg19UCSC Ensembl
Innerchr9:120648653..120656357hg18UCSC Ensembl
Outerchr9:120648453..120656557hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg388105
hg198105
hg188105
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3302903
Supporting Variants
SamplesNA18522
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7737240
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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