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nsv6444576

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:820

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 131 SVs from 33 studies. See in: genome view    
    Submitted genomic87,857,294-87,858,113Question Mark
    Overlapping variant regions from other studies: 131 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):90,472,209-90,473,028Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6444576Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr987,857,29487,858,113
    nsv6444576RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr990,472,20990,473,028

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18190379deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18190379Submitted genomicNC_000009.12:g.878
    57294_87858113del
    GRCh38 (hg38)NC_000009.12Chr987,857,29487,858,113
    nssv18190379RemappedPerfectNC_000009.11:g.904
    72209_90473028del
    GRCh37.p13First PassNC_000009.11Chr990,472,20990,473,028

    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)
    nssv18190379<0.001239228
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