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nsv6382898

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,206

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 140 SVs from 31 studies. See in: genome view    
    Submitted genomic73,740,833-73,747,038Question Mark
    Overlapping variant regions from other studies: 140 SVs from 31 studies. See in: genome view    
    Remapped(Score: Perfect):74,606,550-74,612,755Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6382898Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr473,740,83373,747,038
    nsv6382898RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr474,606,55074,612,755

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18120922deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18120922Submitted genomicNC_000004.12:g.737
    40833_73747038del
    GRCh38 (hg38)NC_000004.12Chr473,740,83373,747,038
    nssv18120922RemappedPerfectNC_000004.11:g.746
    06550_74612755del
    GRCh37.p13First PassNC_000004.11Chr474,606,55074,612,755

    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)
    nssv18120922<0.001139178
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