A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7765159



Internal ID13246608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109149979..109149980hg38UCSC Ensembl
Innerchr9:109149957..109150002hg38UCSC Ensembl
Outerchr9:109149956..109150003hg38UCSC Ensembl
chr9:111912259..111912260hg19UCSC Ensembl
Innerchr9:111912237..111912282hg19UCSC Ensembl
Outerchr9:111912236..111912283hg19UCSC Ensembl
chr9:110952080..110952081hg18UCSC Ensembl
Innerchr9:110952103..110952058hg18UCSC Ensembl
Outerchr9:110952057..110952104hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38292
hg19292
hg18292
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3307202
Supporting Variants
SamplesNA12812
Known GenesFRRS1L
MethodSequencing
Analysis
PlatformRoche 454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7765159
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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