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nsv6533650

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,429

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 143 SVs from 27 studies. See in: genome view    
    Submitted genomic36,333,594-36,335,022Question Mark
    Overlapping variant regions from other studies: 143 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):36,824,496-36,825,924Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6533650Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1936,333,59436,335,022
    nsv6533650RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1936,824,49636,825,924

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18046351deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18046351Submitted genomicNC_000019.10:g.363
    33594_36335022del
    GRCh38 (hg38)NC_000019.10Chr1936,333,59436,335,022
    nssv18046351RemappedPerfectNC_000019.9:g.3682
    4496_36825924del
    GRCh37.p13First PassNC_000019.9Chr1936,824,49636,825,924

    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)
    nssv18046351<0.001138224
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