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nsv7058720

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,924,319

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 5821 SVs from 129 studies. See in: genome view    
    Submitted genomic21,529,628-23,453,946Question Mark
    Overlapping variant regions from other studies: 5821 SVs from 129 studies. See in: genome view    
    Remapped(Score: Perfect):21,540,949-23,465,267Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7058720Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1621,529,62823,453,946
    nsv7058720RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1621,540,94923,465,267

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756420inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756420Submitted genomicNC_000016.10:g.215
    29628_23453946inv
    GRCh38 (hg38)NC_000016.10Chr1621,529,62823,453,946
    nssv18756420RemappedPerfectNC_000016.9:g.2154
    0949_23465267inv
    GRCh37.p13First PassNC_000016.9Chr1621,540,94923,465,267

    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)
    nssv187564204e-061276268
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