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nsv5965314

  • 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: 96 SVs from 19 studies. See in: genome view    
Submitted genomic95,758,002-95,758,002Question Mark
Overlapping variant regions from other studies: 96 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):97,517,759-97,517,759Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5965314Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1095,758,00295,758,002
nsv5965314RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1097,517,75997,517,759

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17351459insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17351459Submitted genomicNC_000010.11:g.957
58002_95758003ins1
52
GRCh38 (hg38)NC_000010.11Chr1095,758,00295,758,002
nssv17351459RemappedPerfectNC_000010.10:g.975
17759_97517760ins1
52
GRCh37.p13First PassNC_000010.10Chr1097,517,75997,517,759

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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