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nsv7066606

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:489,814

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1687 SVs from 75 studies. See in: genome view    
    Submitted genomic67,967,096-68,456,909Question Mark
    Overlapping variant regions from other studies: 1687 SVs from 75 studies. See in: genome view    
    Remapped(Score: Perfect):69,726,853-70,216,666Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7066606Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1067,967,09668,456,909
    nsv7066606RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1069,726,85370,216,666

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18748757inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18748757Submitted genomicNC_000010.11:g.679
    67096_68456909inv
    GRCh38 (hg38)NC_000010.11Chr1067,967,09668,456,909
    nssv18748757RemappedPerfectNC_000010.10:g.697
    26853_70216666inv
    GRCh37.p13First PassNC_000010.10Chr1069,726,85370,216,666

    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)
    nssv187487574e-061276268
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