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nsv7012434

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:475

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 108 SVs from 30 studies. See in: genome view    
    Submitted genomic45,176,783-45,177,257Question Mark
    Overlapping variant regions from other studies: 108 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):45,680,041-45,680,515Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7012434Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1945,176,78345,177,257
    nsv7012434RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1945,680,04145,680,515

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18638862duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18638862Submitted genomicNC_000019.10:g.451
    76783_45177257dup
    GRCh38 (hg38)NC_000019.10Chr1945,176,78345,177,257
    nssv18638862RemappedPerfectNC_000019.9:g.4568
    0041_45680515dup
    GRCh37.p13First PassNC_000019.9Chr1945,680,04145,680,515

    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)
    nssv18638862<0.00136245516
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