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nsv5554080

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,384

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 106 SVs from 24 studies. See in: genome view    
Submitted genomic70,397,332-70,398,715Question Mark
Overlapping variant regions from other studies: 109 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):73,012,248-73,013,631Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5554080Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr970,397,33270,398,715
nsv5554080RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr973,012,24873,013,631

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17023303sequence alterationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv17023303Submitted genomicGRCh38 (hg38)NC_000009.12Chr970,397,33270,398,715
nssv17023303RemappedPerfectGRCh37.p13First PassNC_000009.11Chr973,012,24873,013,631

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)
nssv17023303<0.00126404
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