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nsv821663

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,471

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 378 SVs from 51 studies. See in: genome view    
Remapped(Score: Perfect):62,921,555-62,923,025Question Mark
Overlapping variant regions from other studies: 233 SVs from 45 studies. See in: genome view    
Remapped(Score: Perfect):66,577,379-66,578,849Question Mark
Overlapping variant regions from other studies: 16 SVs from 3 studies. See in: genome view    
Submitted genomic64,258,651-64,260,121Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv821663RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr962,921,55562,923,025
nsv821663RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr966,577,37966,578,849
nsv821663Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000009.9Chr964,258,65164,260,121

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1421236copy number lossROMAProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv1421236RemappedPerfectNC_000009.12:g.(?_
62921555)_(6292302
5_?)del
GRCh38.p12First PassNC_000009.12Chr962,921,55562,923,025
nssv1421236RemappedPerfectNC_000009.11:g.(?_
66577379)_(6657884
9_?)del
GRCh37.p13First PassNC_000009.11Chr966,577,37966,578,849
nssv1421236Submitted genomicNC_000009.9:g.(?_6
4258651)_(64260121
_?)del
NCBI35 (hg17)NC_000009.9Chr964,258,65164,260,121

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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