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nsv6457381

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:355,983

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1266 SVs from 74 studies. See in: genome view    
    Submitted genomic98,057,072-98,413,054Question Mark
    Overlapping variant regions from other studies: 1267 SVs from 74 studies. See in: genome view    
    Remapped(Score: Perfect):97,927,800-98,283,783Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6457381Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1198,057,07298,413,054
    nsv6457381RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1197,927,80098,283,783

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17995877deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17995877Submitted genomicNC_000011.10:g.980
    57072_98413054del
    GRCh38 (hg38)NC_000011.10Chr1198,057,07298,413,054
    nssv17995877RemappedPerfectNC_000011.9:g.9792
    7800_98283783del
    GRCh37.p13First PassNC_000011.9Chr1197,927,80098,283,783

    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)
    nssv17995877<0.001138790
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