A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3306684



Internal ID14806946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26751419..26751420hg38UCSC Ensembl
Innerchr10:26751391..26751448hg38UCSC Ensembl
Outerchr10:26751390..26751449hg38UCSC Ensembl
chr10:27040348..27040349hg19UCSC Ensembl
Innerchr10:27040320..27040377hg19UCSC Ensembl
Outerchr10:27040319..27040378hg19UCSC Ensembl
chr10:27080354..27080355hg18UCSC Ensembl
Innerchr10:27080383..27080326hg18UCSC Ensembl
Outerchr10:27080325..27080384hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7744704, essv7757132, essv7749887, essv7757575, essv7761857, essv7751361, essv7749766, essv7762648, essv7755343, essv7749254, essv7755022, essv7756774, essv7742100, essv7754327, essv7760822
SamplesNA19190, NA12155, NA18550, NA18582, NA12156, NA12003, NA18856, NA18523, NA18570, NA18576, NA18608, NA19108, NA19093, NA18609, NA12154
Known GenesABI1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3306684
Frequency
Sample Size185
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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