A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697093



Internal ID15103295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63112860..63115458hg38UCSC Ensembl
Innerchr9:63113860..63114458hg38UCSC Ensembl
Outerchr9:63111860..63116458hg38UCSC Ensembl
chr9:67017832..67020430hg19UCSC Ensembl
Innerchr9:67018832..67019430hg19UCSC Ensembl
Outerchr9:67016832..67021430hg19UCSC Ensembl
chr9:66757652..66760250hg18UCSC Ensembl
Innerchr9:66758652..66759250hg18UCSC Ensembl
Outerchr9:66756652..66761250hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg382599
hg192599
hg182599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3389528
Supporting Variants
SamplesNA19240
Known GenesLOC286297
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697093
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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