A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3352463



Internal ID14852727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44294998..44295996hg38UCSC Ensembl
Innerchr10:44294997..44295997hg38UCSC Ensembl
Outerchr10:44293998..44296996hg38UCSC Ensembl
chr10:44790446..44791444hg19UCSC Ensembl
Innerchr10:44790445..44791445hg19UCSC Ensembl
Outerchr10:44789446..44792444hg19UCSC Ensembl
chr10:44110452..44111450hg18UCSC Ensembl
Innerchr10:44111451..44110451hg18UCSC Ensembl
Outerchr10:44109452..44112450hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38999
hg19999
hg18999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8688052
SamplesNA19239
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3352463
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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