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nsv6789471

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:456

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 99 SVs from 17 studies. See in: genome view    
    Submitted genomic75,493,728-75,494,183Question Mark
    Overlapping variant regions from other studies: 99 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):76,203,444-76,203,899Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6789471Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr675,493,72875,494,183
    nsv6789471RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr676,203,44476,203,899

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18528204deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18528204Submitted genomicNC_000006.12:g.754
    93728_75494183del
    GRCh38 (hg38)NC_000006.12Chr675,493,72875,494,183
    nssv18528204RemappedPerfectNC_000006.11:g.762
    03444_76203899del
    GRCh37.p13First PassNC_000006.11Chr676,203,44476,203,899

    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)
    nssv185282041.1e-053265840
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