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nsv6422973

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:32,794

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 387 SVs from 49 studies. See in: genome view    
    Submitted genomic21,205,136-21,237,929Question Mark
    Overlapping variant regions from other studies: 393 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):21,205,135-21,237,928Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6422973Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr921,205,13621,237,929
    nsv6422973RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr921,205,13521,237,928

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18176485deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18176485Submitted genomicNC_000009.12:g.212
    05136_21237929del
    GRCh38 (hg38)NC_000009.12Chr921,205,13621,237,929
    nssv18176485RemappedPerfectNC_000009.11:g.212
    05135_21237928del
    GRCh37.p13First PassNC_000009.11Chr921,205,13521,237,928

    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)
    nssv18176485<0.001139226
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