A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3414282



Internal ID15261241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117581121..117581140hg38UCSC Ensembl
Innerchr10:117581117..117581144hg38UCSC Ensembl
Outerchr10:117581098..117581163hg38UCSC Ensembl
chr10:119340632..119340651hg19UCSC Ensembl
Innerchr10:119340628..119340655hg19UCSC Ensembl
Outerchr10:119340609..119340674hg19UCSC Ensembl
chr10:119330622..119330641hg18UCSC Ensembl
Innerchr10:119330645..119330618hg18UCSC Ensembl
Outerchr10:119330599..119330664hg18UCSC Ensembl
Cytoband10q26.11
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 Variantsessv9649802
SamplesNA12874
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3414282
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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