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nsv5562338

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 177 SVs from 19 studies. See in: genome view    
Submitted genomic54,296,257-54,296,308Question Mark
Overlapping variant regions from other studies: 177 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):51,822,627-51,822,678Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5562338Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1854,296,25754,296,308
nsv5562338RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1851,822,62751,822,678

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17718317line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17718317Submitted genomicNC_000018.10:g.542
96257_54296308ins6
019
GRCh38 (hg38)NC_000018.10Chr1854,296,25754,296,308
nssv17718317RemappedPerfectNC_000018.9:g.5182
2627_51822678ins60
19
GRCh37.p13First PassNC_000018.9Chr1851,822,62751,822,678

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)
nssv17718317<0.00116404
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