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nsv5450789

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:74

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 234 SVs from 44 studies. See in: genome view    
Submitted genomic196,478,836-196,478,909Question Mark
Overlapping variant regions from other studies: 234 SVs from 44 studies. See in: genome view    
Remapped(Score: Perfect):196,205,707-196,205,780Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5450789Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3196,478,836196,478,909
nsv5450789RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3196,205,707196,205,780

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16944261duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16944261Submitted genomicNC_000003.12:g.196
478836_196478909du
p
GRCh38 (hg38)NC_000003.12Chr3196,478,836196,478,909
nssv16944261RemappedPerfectNC_000003.11:g.196
205707_196205780du
p
GRCh37.p13First PassNC_000003.11Chr3196,205,707196,205,780

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)
nssv169442610.005296392
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