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nsv951589

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:83,100

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1767 SVs from 86 studies. See in: genome view    
Remapped(Score: Perfect):46,991,862-47,074,961Question Mark
Overlapping variant regions from other studies: 252 SVs from 51 studies. See in: genome view    
Submitted genomic48,664,401-48,747,500Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv951589RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1046,991,86247,074,961
nsv951589Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000010.10Chr1048,664,40148,747,500

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv2997980deletionSAMN01096093SequencingRead depth9,109

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv2997980RemappedPerfectNC_000010.11:g.(46
991862_?)_(?_47074
961)del
GRCh38.p12First PassNC_000010.11Chr1046,991,86247,074,961
nssv2997980Submitted genomicNC_000010.10:g.(48
664401_?)_(?_48747
500)del
GRCh37 (hg19)NC_000010.10Chr1048,664,40148,747,500

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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