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nsv6396289

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:83,521

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 307 SVs from 60 studies. See in: genome view    
    Submitted genomic26,236,593-26,320,113Question Mark
    Overlapping variant regions from other studies: 307 SVs from 60 studies. See in: genome view    
    Remapped(Score: Perfect):26,236,821-26,320,341Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6396289Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr626,236,59326,320,113
    nsv6396289RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr626,236,82126,320,341

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18140734deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18140734Submitted genomicNC_000006.12:g.262
    36593_26320113del
    GRCh38 (hg38)NC_000006.12Chr626,236,59326,320,113
    nssv18140734RemappedPerfectNC_000006.11:g.262
    36821_26320341del
    GRCh37.p13First PassNC_000006.11Chr626,236,82126,320,341

    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)
    nssv18140734<0.001139210
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