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nsv5490534

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:186,593

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 719 SVs from 77 studies. See in: genome view    
Submitted genomic38,498,789-38,685,381Question Mark
Overlapping variant regions from other studies: 732 SVs from 79 studies. See in: genome view    
Remapped(Score: Perfect):38,498,786-38,685,378Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5490534Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr938,498,78938,685,381
nsv5490534RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr938,498,78638,685,378

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17022900deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17022900Submitted genomicNC_000009.12:g.384
98789_38685381del
GRCh38 (hg38)NC_000009.12Chr938,498,78938,685,381
nssv17022900RemappedPerfectNC_000009.11:g.384
98786_38685378del
GRCh37.p13First PassNC_000009.11Chr938,498,78638,685,378

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)
nssv17022900<0.00126404
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