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nsv6643556

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,988

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 111 SVs from 19 studies. See in: genome view    
    Submitted genomic163,195,956-163,199,943Question Mark
    Overlapping variant regions from other studies: 115 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):163,165,746-163,169,733Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6643556Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1163,195,956163,199,943
    nsv6643556RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1163,165,746163,169,733

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18364475deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18364475Submitted genomicNC_000001.11:g.163
    195956_163199943de
    l
    GRCh38 (hg38)NC_000001.11Chr1163,195,956163,199,943
    nssv18364475RemappedPerfectNC_000001.10:g.163
    165746_163169733de
    l
    GRCh37.p13First PassNC_000001.10Chr1163,165,746163,169,733

    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)
    nssv183644754e-061276074
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