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nsv6617508

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,433

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 79 SVs from 22 studies. See in: genome view    
    Submitted genomic45,885,822-45,888,254Question Mark
    Overlapping variant regions from other studies: 79 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):45,925,421-45,927,853Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6617508Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr745,885,82245,888,254
    nsv6617508RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr745,925,42145,927,853

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18155086deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18155086Submitted genomicNC_000007.14:g.458
    85822_45888254del
    GRCh38 (hg38)NC_000007.14Chr745,885,82245,888,254
    nssv18155086RemappedPerfectNC_000007.13:g.459
    25421_45927853del
    GRCh37.p13First PassNC_000007.13Chr745,925,42145,927,853

    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)
    nssv18155086<0.001138488
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