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nsv5616926

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 87 SVs from 18 studies. See in: genome view    
Submitted genomic85,817,544-85,817,544Question Mark
Overlapping variant regions from other studies: 87 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):86,044,667-86,044,667Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5616926Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr285,817,54485,817,544
nsv5616926RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr286,044,66786,044,667

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv17115627insertionHG02587SequencingSequence alignment2,330

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17115627Submitted genomicNC_000002.12:g.858
17544_85817545ins3
72
GRCh38 (hg38)NC_000002.12Chr285,817,54485,817,544
nssv17115627RemappedPerfectNC_000002.11:g.860
44667_86044668ins3
72
GRCh37.p13First PassNC_000002.11Chr286,044,66786,044,667

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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