A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8696809



Internal ID13659241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64455060..64480775hg38UCSC Ensembl
Innerchr9:64456060..64479774hg38UCSC Ensembl
Outerchr9:64454060..64481774hg38UCSC Ensembl
chr9:43016156..43041854hg19UCSC Ensembl
Innerchr9:43017156..43040854hg19UCSC Ensembl
Outerchr9:43015156..43042854hg19UCSC Ensembl
chr9:43006152..43031850hg18UCSC Ensembl
Innerchr9:43007152..43030850hg18UCSC Ensembl
Outerchr9:43005152..43032850hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3825716
hg1925699
hg1825699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3417376
Supporting Variants
SamplesNA12878
Known GenesFAM95B1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8696809
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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