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nsv5450407

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,604

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 103 SVs from 22 studies. See in: genome view    
Submitted genomic119,490,648-119,492,251Question Mark
Overlapping variant regions from other studies: 103 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):119,209,495-119,211,098Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5450407Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3119,490,648119,492,251
nsv5450407RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3119,209,495119,211,098

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16939451deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16939451Submitted genomicNC_000003.12:g.119
490648_119492251de
l
GRCh38 (hg38)NC_000003.12Chr3119,490,648119,492,251
nssv16939451RemappedPerfectNC_000003.11:g.119
209495_119211098de
l
GRCh37.p13First PassNC_000003.11Chr3119,209,495119,211,098

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)
nssv16939451<0.00116404
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