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nsv5450467

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,470

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 131 SVs from 34 studies. See in: genome view    
Submitted genomic133,480,395-133,495,864Question Mark
Overlapping variant regions from other studies: 131 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):133,199,239-133,214,708Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5450467Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3133,480,395133,495,864
nsv5450467RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3133,199,239133,214,708

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16937767duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16937767Submitted genomicNC_000003.12:g.133
480395_133495864du
p
GRCh38 (hg38)NC_000003.12Chr3133,480,395133,495,864
nssv16937767RemappedPerfectNC_000003.11:g.133
199239_133214708du
p
GRCh37.p13First PassNC_000003.11Chr3133,199,239133,214,708

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)
nssv16937767<0.00126404
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