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nsv7007309

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,159,850

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 6219 SVs from 108 studies. See in: genome view    
    Submitted genomic58,709,678-60,869,527Question Mark
    Overlapping variant regions from other studies: 6220 SVs from 108 studies. See in: genome view    
    Remapped(Score: Perfect):56,376,910-58,536,760Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7007309Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1858,709,67860,869,527
    nsv7007309RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1856,376,91058,536,760

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18634570duplicationSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18634570Submitted genomicNC_000018.10:g.587
    09678_60869527dup
    GRCh38 (hg38)NC_000018.10Chr1858,709,67860,869,527
    nssv18634570RemappedPerfectNC_000018.9:g.5637
    6910_58536760dup
    GRCh37.p13First PassNC_000018.9Chr1856,376,91058,536,760

    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)
    nssv186345704e-061273862
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