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nsv6869562

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:56,869

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 243 SVs from 42 studies. See in: genome view    
    Submitted genomic92,415,436-92,472,304Question Mark
    Overlapping variant regions from other studies: 243 SVs from 42 studies. See in: genome view    
    Remapped(Score: Perfect):95,177,718-95,234,586Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6869562Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr992,415,43692,472,304
    nsv6869562RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr995,177,71895,234,586

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18576663deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18576663Submitted genomicNC_000009.12:g.924
    15436_92472304del
    GRCh38 (hg38)NC_000009.12Chr992,415,43692,472,304
    nssv18576663RemappedPerfectNC_000009.11:g.951
    77718_95234586del
    GRCh37.p13First PassNC_000009.11Chr995,177,71895,234,586

    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)
    nssv185766637e-062276234
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