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nsv7058013

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,845,353

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 6061 SVs from 106 studies. See in: genome view    
    Submitted genomic243,978,689-245,824,041Question Mark
    Overlapping variant regions from other studies: 6064 SVs from 106 studies. See in: genome view    
    Remapped(Score: Perfect):244,141,991-245,987,343Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7058013Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1243,978,689245,824,041
    nsv7058013RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1244,141,991245,987,343

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18759444inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18759444Submitted genomicNC_000001.11:g.243
    978689_245824041in
    v
    GRCh38 (hg38)NC_000001.11Chr1243,978,689245,824,041
    nssv18759444RemappedPerfectNC_000001.10:g.244
    141991_245987343in
    v
    GRCh37.p13First PassNC_000001.10Chr1244,141,991245,987,343

    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)
    nssv187594444e-061276268
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