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nsv7046870

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:26

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 173 SVs from 27 studies. See in: genome view    
    Submitted genomic239,800,417-239,800,442Question Mark
    Overlapping variant regions from other studies: 176 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):239,963,717-239,963,742Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7046870Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1239,800,417239,800,442
    nsv7046870RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1239,963,717239,963,742

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759394inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759394Submitted genomicNC_000001.11:g.239
    800417_239800442in
    v
    GRCh38 (hg38)NC_000001.11Chr1239,800,417239,800,442
    nssv18759394RemappedPerfectNC_000001.10:g.239
    963717_239963742in
    v
    GRCh37.p13First PassNC_000001.10Chr1239,963,717239,963,742

    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)
    nssv187593944e-061276160
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