A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3359960



Internal ID15206939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43696098..43696996hg38UCSC Ensembl
Innerchr10:43696097..43696997hg38UCSC Ensembl
Outerchr10:43695098..43697996hg38UCSC Ensembl
chr10:44191546..44192444hg19UCSC Ensembl
Innerchr10:44191545..44192445hg19UCSC Ensembl
Outerchr10:44190546..44193444hg19UCSC Ensembl
chr10:43511552..43512450hg18UCSC Ensembl
Innerchr10:43512451..43511551hg18UCSC Ensembl
Outerchr10:43510552..43513450hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38899
hg19899
hg18899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8688051
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3359960
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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