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nsv6461442

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:875

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 109 SVs from 25 studies. See in: genome view    
    Submitted genomic53,378,053-53,378,927Question Mark
    Overlapping variant regions from other studies: 109 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):53,771,837-53,772,711Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6461442Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1253,378,05353,378,927
    nsv6461442RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1253,771,83753,772,711

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18001451deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18001451Submitted genomicNC_000012.12:g.533
    78053_53378927del
    GRCh38 (hg38)NC_000012.12Chr1253,378,05353,378,927
    nssv18001451RemappedPerfectNC_000012.11:g.537
    71837_53772711del
    GRCh37.p13First PassNC_000012.11Chr1253,771,83753,772,711

    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)
    nssv18001451<0.001436680
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