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nsv3112721

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,582

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 251 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):82,369,676-82,378,257Question Mark
Overlapping variant regions from other studies: 251 SVs from 46 studies. See in: genome view    
Submitted genomic80,327,552-80,336,133Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv3112721RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1782,369,67682,378,257
nsv3112721Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000017.10Chr1780,327,55280,336,133

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv14098884deletionsample138Oligo aCGHProbe signal intensity112

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv14098884RemappedPerfectNC_000017.11:g.(?_
82369676)_(8237825
7_?)del
GRCh38.p12First PassNC_000017.11Chr1782,369,67682,378,257
nssv14098884Submitted genomicNC_000017.10:g.(?_
80327552)_(8033613
3_?)del
GRCh37 (hg19)NC_000017.10Chr1780,327,55280,336,133

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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