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nsv6872815

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:649

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 89 SVs from 18 studies. See in: genome view    
    Submitted genomic111,557,667-111,558,315Question Mark
    Overlapping variant regions from other studies: 89 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):114,319,947-114,320,595Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6872815Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9111,557,667111,558,315
    nsv6872815RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9114,319,947114,320,595

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18734128duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18734128Submitted genomicNC_000009.12:g.111
    557667_111558315du
    p
    GRCh38 (hg38)NC_000009.12Chr9111,557,667111,558,315
    nssv18734128RemappedPerfectNC_000009.11:g.114
    319947_114320595du
    p
    GRCh37.p13First PassNC_000009.11Chr9114,319,947114,320,595

    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)
    nssv187341284e-061251056
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