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nsv7075723

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:199,999

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 759 SVs from 78 studies. See in: genome view    
    Submitted genomic52,287,321-52,487,319Question Mark
    Overlapping variant regions from other studies: 759 SVs from 78 studies. See in: genome view    
    Remapped(Score: Perfect):52,861,456-53,061,454Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7075723Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1352,287,32152,487,319
    nsv7075723RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1352,861,45653,061,454

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18753006inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18753006Submitted genomicNC_000013.11:g.522
    87321_52487319inv
    GRCh38 (hg38)NC_000013.11Chr1352,287,32152,487,319
    nssv18753006RemappedPerfectNC_000013.10:g.528
    61456_53061454inv
    GRCh37.p13First PassNC_000013.10Chr1352,861,45653,061,454

    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)
    nssv187530065.7e-0514274350
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