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nsv6643199

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:56,088

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 213 SVs from 26 studies. See in: genome view    
    Submitted genomic163,285,084-163,341,171Question Mark
    Overlapping variant regions from other studies: 217 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):163,254,874-163,310,961Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6643199Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1163,285,084163,341,171
    nsv6643199RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1163,254,874163,310,961

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18362785deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18362785Submitted genomicNC_000001.11:g.163
    285084_163341171de
    l
    GRCh38 (hg38)NC_000001.11Chr1163,285,084163,341,171
    nssv18362785RemappedPerfectNC_000001.10:g.163
    254874_163310961de
    l
    GRCh37.p13First PassNC_000001.10Chr1163,254,874163,310,961

    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)
    nssv183627854e-061276216
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