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nsv6875175

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:121,340

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 415 SVs from 49 studies. See in: genome view    
    Submitted genomic92,337,320-92,458,659Question Mark
    Overlapping variant regions from other studies: 415 SVs from 49 studies. See in: genome view    
    Remapped(Score: Perfect):95,099,602-95,220,941Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6875175Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr992,337,32092,458,659
    nsv6875175RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr995,099,60295,220,941

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18573383deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18573383Submitted genomicNC_000009.12:g.923
    37320_92458659del
    GRCh38 (hg38)NC_000009.12Chr992,337,32092,458,659
    nssv18573383RemappedPerfectNC_000009.11:g.950
    99602_95220941del
    GRCh37.p13First PassNC_000009.11Chr995,099,60295,220,941

    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)
    nssv185733834e-061276096
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