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nsv5491819

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:72

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 81 SVs from 16 studies. See in: genome view    
Submitted genomic121,279,041-121,279,112Question Mark
Overlapping variant regions from other studies: 81 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):124,041,319-124,041,390Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5491819Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9121,279,041121,279,112
nsv5491819RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9124,041,319124,041,390

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17028542deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17028542Submitted genomicNC_000009.12:g.121
279041_121279112de
l
GRCh38 (hg38)NC_000009.12Chr9121,279,041121,279,112
nssv17028542RemappedPerfectNC_000009.11:g.124
041319_124041390de
l
GRCh37.p13First PassNC_000009.11Chr9124,041,319124,041,390

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)
nssv17028542<0.00116404
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