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nsv831374

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:205,373

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 811 SVs from 85 studies. See in: genome view    
Remapped(Score: Perfect):84,191,369-84,396,741Question Mark
Overlapping variant regions from other studies: 811 SVs from 85 studies. See in: genome view    
Remapped(Score: Perfect):85,103,604-85,308,976Question Mark
Overlapping variant regions from other studies: 58 SVs from 6 studies. See in: genome view    
Submitted genomic85,266,159-85,471,531Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv831374RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr884,191,36984,396,741
nsv831374RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr885,103,60485,308,976
nsv831374Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000008.9Chr885,266,15985,471,531

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1447237copy number lossBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1447237RemappedPerfectNC_000008.11:g.(84
191369_?)_(?_84396
741)del
GRCh38.p12First PassNC_000008.11Chr884,191,36984,396,741
nssv1447237RemappedPerfectNC_000008.10:g.(85
103604_?)_(?_85308
976)del
GRCh37.p13First PassNC_000008.10Chr885,103,60485,308,976
nssv1447237Submitted genomicNC_000008.9:g.(852
66159_?)_(?_854715
31)del
NCBI35 (hg17)NC_000008.9Chr885,266,15985,471,531

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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