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nsv833860

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:132,107

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 469 SVs from 57 studies. See in: genome view    
Remapped(Score: Perfect):49,286,685-49,418,791Question Mark
Overlapping variant regions from other studies: 469 SVs from 57 studies. See in: genome view    
Remapped(Score: Perfect):49,789,942-49,922,048Question Mark
Overlapping variant regions from other studies: 14 SVs from 2 studies. See in: genome view    
Submitted genomic54,481,754-54,613,860Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv833860RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000019.10Chr1949,286,68549,418,791
nsv833860RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1949,789,94249,922,048
nsv833860Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000019.8Chr1954,481,75454,613,860

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1454789copy number lossBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1454789RemappedPerfectNC_000019.10:g.(49
286685_?)_(?_49418
791)del
GRCh38.p12First PassNC_000019.10Chr1949,286,68549,418,791
nssv1454789RemappedPerfectNC_000019.9:g.(497
89942_?)_(?_499220
48)del
GRCh37.p13First PassNC_000019.9Chr1949,789,94249,922,048
nssv1454789Submitted genomicNC_000019.8:g.(544
81754_?)_(?_546138
60)del
NCBI35 (hg17)NC_000019.8Chr1954,481,75454,613,860

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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