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nsv5453818

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:88

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 94 SVs from 20 studies. See in: genome view    
Submitted genomic133,444,798-133,444,885Question Mark
Overlapping variant regions from other studies: 94 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):133,163,642-133,163,729Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5453818Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3133,444,798133,444,885
nsv5453818RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3133,163,642133,163,729

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16937763duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16937763Submitted genomicNC_000003.12:g.133
444798_133444885du
p
GRCh38 (hg38)NC_000003.12Chr3133,444,798133,444,885
nssv16937763RemappedPerfectNC_000003.11:g.133
163642_133163729du
p
GRCh37.p13First PassNC_000003.11Chr3133,163,642133,163,729

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)
nssv16937763<0.00126404
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