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nsv954904

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:53,700

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 273 SVs from 50 studies. See in: genome view    
Remapped(Score: Perfect):22,053,808-22,107,507Question Mark
Overlapping variant regions from other studies: 273 SVs from 50 studies. See in: genome view    
Submitted genomic22,380,301-22,434,000Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv954904RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr122,053,80822,107,507
nsv954904Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr122,380,30122,434,000

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv3003153duplicationSAMN01096093SequencingRead depth9,109

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv3003153RemappedPerfectNC_000001.11:g.(22
053808_?)_(?_22107
507)dup
GRCh38.p12First PassNC_000001.11Chr122,053,80822,107,507
nssv3003153Submitted genomicNC_000001.10:g.(22
380301_?)_(?_22434
000)dup
GRCh37 (hg19)NC_000001.10Chr122,380,30122,434,000

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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