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nsv5401850

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:87

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 131 SVs from 23 studies. See in: genome view    
Submitted genomic69,870,386-69,870,472Question Mark
Overlapping variant regions from other studies: 131 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):70,336,069-70,336,155Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5401850Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr169,870,38669,870,472
nsv5401850RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr170,336,06970,336,155

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16904059alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16904059Submitted genomicNC_000001.11:g.698
70386_69870472ins1
52
GRCh38 (hg38)NC_000001.11Chr169,870,38669,870,472
nssv16904059RemappedPerfectNC_000001.10:g.703
36069_70336155ins1
52
GRCh37.p13First PassNC_000001.10Chr170,336,06970,336,155

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)
nssv16904059<0.00116404
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