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nsv5489451

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:37,895

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 217 SVs from 37 studies. See in: genome view    
Submitted genomic98,071,724-98,109,618Question Mark
Overlapping variant regions from other studies: 217 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):100,834,006-100,871,900Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5489451Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr998,071,72498,109,618
nsv5489451RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9100,834,006100,871,900

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17026872deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17026872Submitted genomicNC_000009.12:g.980
71724_98109618del
GRCh38 (hg38)NC_000009.12Chr998,071,72498,109,618
nssv17026872RemappedPerfectNC_000009.11:g.100
834006_100871900de
l
GRCh37.p13First PassNC_000009.11Chr9100,834,006100,871,900

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17026872<0.00116404
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