nsv448277

  • Variant Calls:1
  • Validation:Yes
  • Region Size:86

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 5 SVs from 1 studies. See in: genome view    
Remapped(Score: Perfect):26,231,002-26,231,087Question Mark
Overlapping variant regions from other studies: 5 SVs from 1 studies. See in: genome view    
Submitted genomic26,367,947-26,368,032Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter StopTransposition
nsv448277RemappedPerfectGRCm38 (mm10)C57BL/6JFirst PassNC_000083.6Chr1726,231,00226,231,087Recipient
nsv448277Submitted genomicMGSCv37 (mm9)NC_000083.5Chr1726,367,94726,368,032Recipient

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls from this Sample
nssv527524mobile element insertionDBA/2JSequencingPaired-end mapping7,367

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nssv527524RemappedPerfectGRCm38 (mm10)C57BL/6JFirst PassNC_000083.6Chr1726,231,00226,231,087
nssv527524Submitted genomicMGSCv37 (mm9)NC_000083.5Chr1726,367,94726,368,032

Validation Information

Variant Call IDExperiment IDSample IDMethodAnalysisResult
nssv5275243DBA/2JSequencingSequence alignmentPass

There is no genotype information for this variant