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nsv6523224

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,661

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 96 SVs from 20 studies. See in: genome view    
    Submitted genomic41,217,867-41,221,527Question Mark
    Overlapping variant regions from other studies: 96 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):41,723,772-41,727,432Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6523224Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1941,217,86741,221,527
    nsv6523224RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1941,723,77241,727,432

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18048066deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18048066Submitted genomicNC_000019.10:g.412
    17867_41221527del
    GRCh38 (hg38)NC_000019.10Chr1941,217,86741,221,527
    nssv18048066RemappedPerfectNC_000019.9:g.4172
    3772_41727432del
    GRCh37.p13First PassNC_000019.9Chr1941,723,77241,727,432

    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)
    nssv18048066<0.001139008
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