U.S. flag

An official website of the United States government

nsv6958411

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,274

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 161 SVs from 30 studies. See in: genome view    
    Submitted genomic75,007,580-75,009,853Question Mark
    Overlapping variant regions from other studies: 161 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):75,299,921-75,302,194Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6958411Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1575,007,58075,009,853
    nsv6958411RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1575,299,92175,302,194

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18398170deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18398170Submitted genomicNC_000015.10:g.750
    07580_75009853del
    GRCh38 (hg38)NC_000015.10Chr1575,007,58075,009,853
    nssv18398170RemappedPerfectNC_000015.9:g.7529
    9921_75302194del
    GRCh37.p13First PassNC_000015.9Chr1575,299,92175,302,194

    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)
    nssv183981704e-061275720
    Support Center