A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8697411



Internal ID15062147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89058017..89060615hg38UCSC Ensembl
Innerchr9:89059017..89059615hg38UCSC Ensembl
Outerchr9:89057017..89061615hg38UCSC Ensembl
chr9:91672932..91675530hg19UCSC Ensembl
Innerchr9:91673932..91674530hg19UCSC Ensembl
Outerchr9:91671932..91676530hg19UCSC Ensembl
chr9:90862752..90865350hg18UCSC Ensembl
Innerchr9:90863752..90864350hg18UCSC Ensembl
Outerchr9:90861752..90866350hg18UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg382599
hg192599
hg182599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3341868
Supporting Variants
SamplesNA19239
Known GenesSHC3
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8697411
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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