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nsv6643251

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,300

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 115 SVs from 23 studies. See in: genome view    
    Submitted genomic160,601,953-160,606,252Question Mark
    Overlapping variant regions from other studies: 119 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):160,571,743-160,576,042Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6643251Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1160,601,953160,606,252
    nsv6643251RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1160,571,743160,576,042

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18362679deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18362679Submitted genomicNC_000001.11:g.160
    601953_160606252de
    l
    GRCh38 (hg38)NC_000001.11Chr1160,601,953160,606,252
    nssv18362679RemappedPerfectNC_000001.10:g.160
    571743_160576042de
    l
    GRCh37.p13First PassNC_000001.10Chr1160,571,743160,576,042

    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)
    nssv183626792.1e-056275760
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