esv277499

  • Variant Calls:1
  • Validation:Not tested
  • Region Size:2

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):77,744,239-77,744,240Question Mark
Overlapping variant regions from other studies: 5 SVs from 1 studies. See in: genome view    
Submitted genomic78,144,046-78,144,047Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
esv277499RemappedPerfectGRCm38 (mm10)C57BL/6JFirst PassNC_000080.6Chr1477,744,23977,744,240
esv277499Submitted genomicMGSCv37 (mm9)NC_000080.5Chr1478,144,04678,144,047

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv2619681insertionBALBcJSequencingPaired-end mapping25,702

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv2619681RemappedPerfectGRCm38 (mm10)C57BL/6JFirst PassNC_000080.6Chr1477,744,19777,744,30877,744,19777,744,308
essv2619681Submitted genomicMGSCv37 (mm9)NC_000080.5Chr1478,144,00478,144,11578,144,00478,144,115

No validation data were submitted for this variant

No genotype data were submitted for this variant

Support Center