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nsv5649317

  • 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: 119 SVs from 25 studies. See in: genome view    
Submitted genomic53,898,914-53,898,914Question Mark
Overlapping variant regions from other studies: 118 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):54,402,168-54,402,168Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5649317Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1953,898,91453,898,914
nsv5649317RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1954,402,16854,402,168

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv17106069insertionSAMN00006579SequencingSequence alignment23,265

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17106069Submitted genomicNC_000019.10:g.538
98914_53898915ins9
0
GRCh38 (hg38)NC_000019.10Chr1953,898,91453,898,914
nssv17106069RemappedPerfectNC_000019.9:g.5440
2168_54402169ins90
GRCh37.p13First PassNC_000019.9Chr1954,402,16854,402,168

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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