nsv499839

  • Variant Calls:1
  • Validation:Not tested
  • Region Size:69,863

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 11 SVs from 3 studies. See in: genome view    
Remapped(Score: Good):101,372,311-101,442,173Question Mark
Overlapping variant regions from other studies: 11 SVs from 3 studies. See in: genome view    
Remapped(Score: Good):100,834,945-100,904,807Question Mark
Submitted genomic101,286,296-101,355,496Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv499839RemappedGoodGRCm38 (mm10)C57BL/6JFirst PassNC_000076.6Chr10101,372,311101,442,173
nsv499839RemappedGoodMGSCv37 (mm9)C57BL/6JFirst PassNC_000076.5Chr10100,834,945100,904,807
nsv499839Submitted genomicMGSCv34NC_000076.2Chr10101,286,296101,355,496

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv604873copy number losswild_6Oligo aCGHProbe signal intensity567

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv604873RemappedGoodGRCm38 (mm10)C57BL/6JFirst PassNC_000076.6Chr10101,367,500101,367,500101,452,224101,452,224
nssv604873RemappedGoodMGSCv37 (mm9)C57BL/6JFirst PassNC_000076.5Chr10100,830,134100,830,134100,914,858100,914,858
nssv604873Submitted genomicMGSCv34NC_000076.2Chr10101,281,485101,286,296101,355,496101,364,888

No validation data were submitted for this variant

No genotype data were submitted for this variant

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