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nsv6796085

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,319

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 70 SVs from 12 studies. See in: genome view    
    Submitted genomic150,376,027-150,379,345Question Mark
    Overlapping variant regions from other studies: 70 SVs from 12 studies. See in: genome view    
    Remapped(Score: Perfect):149,755,590-149,758,908Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6796085Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5150,376,027150,379,345
    nsv6796085RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5149,755,590149,758,908

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18507347deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18507347Submitted genomicNC_000005.10:g.150
    376027_150379345de
    l
    GRCh38 (hg38)NC_000005.10Chr5150,376,027150,379,345
    nssv18507347RemappedPerfectNC_000005.9:g.1497
    55590_149758908del
    GRCh37.p13First PassNC_000005.9Chr5149,755,590149,758,908

    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)
    nssv185073474e-061275514
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