A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3447679



Internal ID15294628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17709955..17709974hg38UCSC Ensembl
Innerchr10:17709951..17709978hg38UCSC Ensembl
Outerchr10:17709932..17709997hg38UCSC Ensembl
chr10:17751954..17751973hg19UCSC Ensembl
Innerchr10:17751950..17751977hg19UCSC Ensembl
Outerchr10:17751931..17751996hg19UCSC Ensembl
chr10:17791960..17791979hg18UCSC Ensembl
Innerchr10:17791983..17791956hg18UCSC Ensembl
Outerchr10:17791937..17792002hg18UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9646147
SamplesNA12287
Known GenesSTAM
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3447679
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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