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nsv1128589

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,901

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 231 SVs from 58 studies. See in: genome view    
Remapped(Score: Perfect):16,506,105-16,517,005Question Mark
Overlapping variant regions from other studies: 231 SVs from 58 studies. See in: genome view    
Submitted genomic16,832,600-16,843,500Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv1128589RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr116,506,10516,517,005
nsv1128589Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr116,832,60016,843,500

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv3960500duplicationKWS1SequencingRead depth and paired-end mapping22,470

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv3960500RemappedPerfectNC_000001.11:g.(16
506105_?)_(?_16517
005)dup
GRCh38.p12First PassNC_000001.11Chr116,506,10516,517,005
nssv3960500Submitted genomicNC_000001.10:g.(16
832600_?)_(?_16843
500)dup
GRCh37 (hg19)NC_000001.10Chr116,832,60016,843,500

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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