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nsv6998003

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:36,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 540 SVs from 69 studies. See in: genome view    
    Submitted genomic84,463,801-84,500,600Question Mark
    Overlapping variant regions from other studies: 540 SVs from 69 studies. See in: genome view    
    Remapped(Score: Perfect):84,497,407-84,534,206Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6998003Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1684,463,80184,500,600
    nsv6998003RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1684,497,40784,534,206

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18405100deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18405100Submitted genomicNC_000016.10:g.844
    63801_84500600del
    GRCh38 (hg38)NC_000016.10Chr1684,463,80184,500,600
    nssv18405100RemappedPerfectNC_000016.9:g.8449
    7407_84534206del
    GRCh37.p13First PassNC_000016.9Chr1684,497,40784,534,206

    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)
    nssv184051004e-061263664
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