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nsv7050592

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,673,116

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 8436 SVs from 105 studies. See in: genome view    
    Submitted genomic181,219,378-183,892,493Question Mark
    Overlapping variant regions from other studies: 8436 SVs from 105 studies. See in: genome view    
    Remapped(Score: Perfect):182,140,531-184,813,646Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7050592Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4181,219,378183,892,493
    nsv7050592RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4182,140,531184,813,646

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18773342inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18773342Submitted genomicNC_000004.12:g.181
    219378_183892493in
    v
    GRCh38 (hg38)NC_000004.12Chr4181,219,378183,892,493
    nssv18773342RemappedPerfectNC_000004.11:g.182
    140531_184813646in
    v
    GRCh37.p13First PassNC_000004.11Chr4182,140,531184,813,646

    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)
    nssv18773342<0.00121271484
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