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nsv6557715

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,971,389

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 16356 SVs from 115 studies. See in: genome view    
    Submitted genomic75,901,418-82,872,806Question Mark
    Overlapping variant regions from other studies: 16356 SVs from 115 studies. See in: genome view    
    Remapped(Score: Perfect):78,516,334-85,487,721Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6557715Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr975,901,41882,872,806
    nsv6557715RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr978,516,33485,487,721

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18281004inversionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18281004Submitted genomicNC_000009.12:g.759
    01418_82872806inv
    GRCh38 (hg38)NC_000009.12Chr975,901,41882,872,806
    nssv18281004RemappedPerfectNC_000009.11:g.785
    16334_85487721inv
    GRCh37.p13First PassNC_000009.11Chr978,516,33485,487,721

    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)
    nssv18281004<0.001139304
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