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nsv6911568

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:10,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 115 SVs from 37 studies. See in: genome view    
    Submitted genomic56,821,001-56,831,800Question Mark
    Overlapping variant regions from other studies: 117 SVs from 37 studies. See in: genome view    
    Remapped(Score: Perfect):56,588,477-56,599,276Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6911568Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1156,821,00156,831,800
    nsv6911568RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1156,588,47756,599,276

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18351718deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18351718Submitted genomicNC_000011.10:g.568
    21001_56831800del
    GRCh38 (hg38)NC_000011.10Chr1156,821,00156,831,800
    nssv18351718RemappedPerfectNC_000011.9:g.5658
    8477_56599276del
    GRCh37.p13First PassNC_000011.9Chr1156,588,47756,599,276

    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)
    nssv183517184e-061276228
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