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nsv5445219

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,755

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 106 SVs from 23 studies. See in: genome view    
Submitted genomic119,545,226-119,548,980Question Mark
Overlapping variant regions from other studies: 106 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):119,264,073-119,267,827Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5445219Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3119,545,226119,548,980
nsv5445219RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3119,264,073119,267,827

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16939455duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16939455Submitted genomicNC_000003.12:g.119
545226_119548980du
p
GRCh38 (hg38)NC_000003.12Chr3119,545,226119,548,980
nssv16939455RemappedPerfectNC_000003.11:g.119
264073_119267827du
p
GRCh37.p13First PassNC_000003.11Chr3119,264,073119,267,827

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)
nssv16939455<0.00126404
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