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nsv6451819

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:151,200

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 451 SVs from 61 studies. See in: genome view    
    Submitted genomic73,597,801-73,749,000Question Mark
    Overlapping variant regions from other studies: 451 SVs from 61 studies. See in: genome view    
    Remapped(Score: Perfect):75,357,559-75,508,758Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6451819Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1073,597,80173,749,000
    nsv6451819RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1075,357,55975,508,758

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18186519duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18186519Submitted genomicNC_000010.11:g.735
    97801_73749000dup
    GRCh38 (hg38)NC_000010.11Chr1073,597,80173,749,000
    nssv18186519RemappedPerfectNC_000010.10:g.753
    57559_75508758dup
    GRCh37.p13First PassNC_000010.10Chr1075,357,55975,508,758

    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)
    nssv18186519<0.0011437212
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