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nsv6374903

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:29,600

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 183 SVs from 40 studies. See in: genome view    
    Submitted genomic122,772,001-122,801,600Question Mark
    Overlapping variant regions from other studies: 183 SVs from 40 studies. See in: genome view    
    Remapped(Score: Perfect):122,490,848-122,520,447Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6374903Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3122,772,001122,801,600
    nsv6374903RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3122,490,848122,520,447

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18207952duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18207952Submitted genomicNC_000003.12:g.122
    772001_122801600du
    p
    GRCh38 (hg38)NC_000003.12Chr3122,772,001122,801,600
    nssv18207952RemappedPerfectNC_000003.11:g.122
    490848_122520447du
    p
    GRCh37.p13First PassNC_000003.11Chr3122,490,848122,520,447

    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)
    nssv18207952<0.0011439242
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