U.S. flag

An official website of the United States government

nsv6992526

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:152,356

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 553 SVs from 58 studies. See in: genome view    
    Submitted genomic72,973,731-73,126,086Question Mark
    Overlapping variant regions from other studies: 553 SVs from 58 studies. See in: genome view    
    Remapped(Score: Perfect):70,969,870-71,122,225Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6992526Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1772,973,73173,126,086
    nsv6992526RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1770,969,87071,122,225

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18414090deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18414090Submitted genomicNC_000017.11:g.729
    73731_73126086del
    GRCh38 (hg38)NC_000017.11Chr1772,973,73173,126,086
    nssv18414090RemappedPerfectNC_000017.10:g.709
    69870_71122225del
    GRCh37.p13First PassNC_000017.10Chr1770,969,87071,122,225

    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)
    nssv184140904e-061276208
    Support Center