U.S. flag

An official website of the United States government

nsv7000238

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:94,111

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 571 SVs from 50 studies. See in: genome view    
    Submitted genomic76,110,470-76,204,580Question Mark
    Overlapping variant regions from other studies: 571 SVs from 50 studies. See in: genome view    
    Remapped(Score: Perfect):73,822,425-73,916,535Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7000238Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1876,110,47076,204,580
    nsv7000238RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1873,822,42573,916,535

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18635023duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18635023Submitted genomicNC_000018.10:g.761
    10470_76204580dup
    GRCh38 (hg38)NC_000018.10Chr1876,110,47076,204,580
    nssv18635023RemappedPerfectNC_000018.9:g.7382
    2425_73916535dup
    GRCh37.p13First PassNC_000018.9Chr1873,822,42573,916,535

    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)
    nssv186350237e-062274490
    Support Center