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nsv6784394

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,788

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 99 SVs from 29 studies. See in: genome view    
    Submitted genomic170,367,087-170,376,874Question Mark
    Overlapping variant regions from other studies: 99 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):169,794,091-169,803,878Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6784394Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5170,367,087170,376,874
    nsv6784394RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5169,794,091169,803,878

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18510540deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18510540Submitted genomicNC_000005.10:g.170
    367087_170376874de
    l
    GRCh38 (hg38)NC_000005.10Chr5170,367,087170,376,874
    nssv18510540RemappedPerfectNC_000005.9:g.1697
    94091_169803878del
    GRCh37.p13First PassNC_000005.9Chr5169,794,091169,803,878

    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)
    nssv185105404e-061276236
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