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nsv7055753

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,628

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 107 SVs from 17 studies. See in: genome view    
    Submitted genomic160,363,397-160,369,024Question Mark
    Overlapping variant regions from other studies: 111 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):160,333,187-160,338,814Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7055753Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1160,363,397160,369,024
    nsv7055753RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1160,333,187160,338,814

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18743743inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18743743Submitted genomicNC_000001.11:g.160
    363397_160369024in
    v
    GRCh38 (hg38)NC_000001.11Chr1160,363,397160,369,024
    nssv18743743RemappedPerfectNC_000001.10:g.160
    333187_160338814in
    v
    GRCh37.p13First PassNC_000001.10Chr1160,333,187160,338,814

    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)
    nssv187437434e-061276268
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