A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3411839



Internal ID14912112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112607256..112607256hg38UCSC Ensembl
Innerchr10:112607255..112607257hg38UCSC Ensembl
Outerchr10:112607206..112607306hg38UCSC Ensembl
chr10:114367015..114367015hg19UCSC Ensembl
Innerchr10:114367014..114367016hg19UCSC Ensembl
Outerchr10:114366965..114367065hg19UCSC Ensembl
chr10:114357005..114357005hg18UCSC Ensembl
Innerchr10:114357006..114357004hg18UCSC Ensembl
Outerchr10:114356955..114357055hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38643
hg19643
hg18643
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8740685
SamplesNA19240
Known GenesVTI1A
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3411839
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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