A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3342799



Internal ID15189784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:41818665..41885263hg38UCSC Ensembl
Innerchr10:41819665..41884263hg38UCSC Ensembl
Outerchr10:41817665..41885273hg38UCSC Ensembl
chr10:42355001..42421544hg19UCSC Ensembl
Innerchr10:42355946..42420544hg19UCSC Ensembl
Outerchr10:42355001..42422544hg19UCSC Ensembl
chr10:41674952..41741550hg18UCSC Ensembl
Innerchr10:41675952..41740550hg18UCSC Ensembl
Outerchr10:41673952..41742550hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg3866599
hg1966544
hg1866599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv402e59
Supporting Variantsessv8688039
SamplesNA19238
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3342799
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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