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esv5381

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:186

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 233 SVs from 57 studies. See in: genome view    
Remapped(Score: Perfect):22,933,524-22,933,709Question Mark
Overlapping variant regions from other studies: 233 SVs from 57 studies. See in: genome view    
Remapped(Score: Perfect):23,507,663-23,507,848Question Mark
Overlapping variant regions from other studies: 96 SVs from 17 studies. See in: genome view    
Submitted genomic22,405,663-22,405,848Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
esv5381RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1322,933,52422,933,709
esv5381RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1323,507,66323,507,848
esv5381Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000013.9Chr1322,405,66322,405,848

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv27822sequence alterationYHSequencingRead depth and paired-end mapping2,682

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrOuter StartOuter Stop
essv27822RemappedPerfectGRCh38.p12First PassNC_000013.11Chr1322,933,52422,933,709
essv27822RemappedPerfectGRCh37.p13First PassNC_000013.10Chr1323,507,66323,507,848
essv27822Submitted genomicNCBI36 (hg18)NC_000013.9Chr1322,405,66322,405,848

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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