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nsv7059660

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,145,256

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3583 SVs from 104 studies. See in: genome view    
    Submitted genomic16,041,448-17,186,703Question Mark
    Overlapping variant regions from other studies: 3583 SVs from 104 studies. See in: genome view    
    Remapped(Score: Perfect):15,944,762-17,090,017Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7059660Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1716,041,44817,186,703
    nsv7059660RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1715,944,76217,090,017

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756168inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756168Submitted genomicNC_000017.11:g.160
    41448_17186703inv
    GRCh38 (hg38)NC_000017.11Chr1716,041,44817,186,703
    nssv18756168RemappedPerfectNC_000017.10:g.159
    44762_17090017inv
    GRCh37.p13First PassNC_000017.10Chr1715,944,76217,090,017

    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)
    nssv187561684e-061276268
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