A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3337356



Internal ID15184343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8106464..8106483hg38UCSC Ensembl
Innerchr10:8106460..8106487hg38UCSC Ensembl
Outerchr10:8106441..8106506hg38UCSC Ensembl
chr10:8148427..8148446hg19UCSC Ensembl
Innerchr10:8148423..8148450hg19UCSC Ensembl
Outerchr10:8148404..8148469hg19UCSC Ensembl
chr10:8188433..8188452hg18UCSC Ensembl
Innerchr10:8188456..8188429hg18UCSC Ensembl
Outerchr10:8188410..8188475hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg386000
hg196000
hg186000
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9645736
SamplesNA12873
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3337356
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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