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nsv6462717

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,400

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 93 SVs from 16 studies. See in: genome view    
    Submitted genomic95,820,901-95,822,300Question Mark
    Overlapping variant regions from other studies: 93 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):95,554,065-95,555,464Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6462717Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1195,820,90195,822,300
    nsv6462717RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1195,554,06595,555,464

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv17995598deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv17995598Submitted genomicNC_000011.10:g.958
    20901_95822300del
    GRCh38 (hg38)NC_000011.10Chr1195,820,90195,822,300
    nssv17995598RemappedPerfectNC_000011.9:g.9555
    4065_95555464del
    GRCh37.p13First PassNC_000011.9Chr1195,554,06595,555,464

    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)
    nssv17995598<0.001139160
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