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nsv6391824

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:754,552

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1899 SVs from 82 studies. See in: genome view    
    Submitted genomic37,603,316-38,357,867Question Mark
    Overlapping variant regions from other studies: 1899 SVs from 82 studies. See in: genome view    
    Remapped(Score: Perfect):37,603,418-38,357,969Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6391824Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr537,603,31638,357,867
    nsv6391824RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr537,603,41838,357,969

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18213439duplicationSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18213439Submitted genomicNC_000005.10:g.376
    03316_38357867dup
    GRCh38 (hg38)NC_000005.10Chr537,603,31638,357,867
    nssv18213439RemappedPerfectNC_000005.9:g.3760
    3418_38357969dup
    GRCh37.p13First PassNC_000005.9Chr537,603,41838,357,969

    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)
    nssv18213439<0.001139294
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