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nsv6842445

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,778

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 161 SVs from 22 studies. See in: genome view    
    Submitted genomic96,304,893-96,310,670Question Mark
    Overlapping variant regions from other studies: 161 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):97,317,121-97,322,898Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6842445Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr896,304,89396,310,670
    nsv6842445RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr897,317,12197,322,898

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18560405deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18560405Submitted genomicNC_000008.11:g.963
    04893_96310670del
    GRCh38 (hg38)NC_000008.11Chr896,304,89396,310,670
    nssv18560405RemappedPerfectNC_000008.10:g.973
    17121_97322898del
    GRCh37.p13First PassNC_000008.10Chr897,317,12197,322,898

    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)
    nssv185604054e-061275848
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