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nsv6519678

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:505,700

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1718 SVs from 80 studies. See in: genome view    
    Submitted genomic72,002,461-72,508,160Question Mark
    Overlapping variant regions from other studies: 1718 SVs from 80 studies. See in: genome view    
    Remapped(Score: Perfect):69,669,696-70,175,395Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6519678Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1872,002,46172,508,160
    nsv6519678RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1869,669,69670,175,395

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18043799deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18043799Submitted genomicNC_000018.10:g.720
    02461_72508160del
    GRCh38 (hg38)NC_000018.10Chr1872,002,46172,508,160
    nssv18043799RemappedPerfectNC_000018.9:g.6966
    9696_70175395del
    GRCh37.p13First PassNC_000018.9Chr1869,669,69670,175,395

    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)
    nssv18043799<0.001138758
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