nsv499832

  • Variant Calls:1
  • Validation:Not tested
  • Region Size:52,365

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 32 SVs from 4 studies. See in: genome view    
Remapped(Score: Perfect):100,573,789-100,626,153Question Mark
Overlapping variant regions from other studies: 32 SVs from 4 studies. See in: genome view    
Remapped(Score: Perfect):100,036,423-100,088,787Question Mark
Submitted genomic100,480,140-100,532,504Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv499832RemappedPerfectGRCm38 (mm10)C57BL/6JFirst PassNC_000076.6Chr10100,573,789100,626,153
nsv499832RemappedPerfectMGSCv37 (mm9)C57BL/6JFirst PassNC_000076.5Chr10100,036,423100,088,787
nsv499832Submitted genomicMGSCv34NC_000076.2Chr10100,480,140100,532,504

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv604833copy number losswild_11Oligo aCGHProbe signal intensity530

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv604833RemappedPerfectGRCm38 (mm10)C57BL/6JFirst PassNC_000076.6Chr10100,567,899100,573,789100,626,153100,633,684
nssv604833RemappedPerfectMGSCv37 (mm9)C57BL/6JFirst PassNC_000076.5Chr10100,030,533100,036,423100,088,787100,096,318
nssv604833Submitted genomicMGSCv34NC_000076.2Chr10100,474,250100,480,140100,532,504100,540,035

No validation data were submitted for this variant

No genotype data were submitted for this variant