nsv820280

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:159

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 187 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):1,206,512-1,206,670Question Mark
Overlapping variant regions from other studies: 187 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):1,156,512-1,156,670Question Mark
Overlapping variant regions from other studies: 170 SVs from 13 studies. See in: genome view    
Submitted genomic1,143,919-1,144,077Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv820280RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000008.11Chr81,206,5121,206,670
nsv820280RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000008.10Chr81,156,5121,156,670
nsv820280Submitted genomicNCBI36 (hg18)NC_000008.9Chr81,143,9191,144,077

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1418892insertionSAMN00002681SequencingPaired-end mapping1,318

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nssv1418892RemappedPerfectNC_000008.11:g.(12
06512_?)_(?_120667
0)ins1371
GRCh38 (hg38)Primary AssemblyFirst PassNC_000008.11Chr81,206,5121,206,670
nssv1418892RemappedPerfectNC_000008.10:g.(11
56512_?)_(?_115667
0)ins1371
GRCh37 (hg19)Primary AssemblyFirst PassNC_000008.10Chr81,156,5121,156,670
nssv1418892Submitted genomicNC_000008.9:g.(114
3919_?)_(?_1144077
)ins1371
NCBI36 (hg18)NC_000008.9Chr81,143,9191,144,077

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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