A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8688091



Internal ID13371229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46420811..46429407hg38UCSC Ensembl
Innerchr10:46421811..46428409hg38UCSC Ensembl
Outerchr10:46419811..46430407hg38UCSC Ensembl
chr10:47120346..47128944hg19UCSC Ensembl
Innerchr10:47121346..47127944hg19UCSC Ensembl
Outerchr10:47119346..47129944hg19UCSC Ensembl
chr10:46540352..46548950hg18UCSC Ensembl
Innerchr10:46541352..46547950hg18UCSC Ensembl
Outerchr10:46539352..46549950hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg388597
hg198599
hg188599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv3434241
Supporting Variants
SamplesNA12892
Known GenesLINC00842
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8688091
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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