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nsv7063878

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,563

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 289 SVs from 46 studies. See in: genome view    
    Submitted genomic36,492,269-36,496,831Question Mark
    Overlapping variant regions from other studies: 83 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):377,019-381,581Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7063878Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1736,492,26936,496,831
    nsv7063878RemappedPerfectGRCh37.p13PATCHESFirst PassNW_003315949.1Chr17|NW_0
    03315949.1
    377,019381,581

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18757230inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18757230Submitted genomicNC_000017.11:g.364
    92269_36496831inv
    GRCh38 (hg38)NC_000017.11Chr1736,492,26936,496,831
    nssv18757230RemappedPerfectNW_003315949.1:g.3
    77019_381581inv
    GRCh37.p13First PassNW_003315949.1Chr17|NW_0
    03315949.1
    377,019381,581

    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)
    nssv187572304e-061276268
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