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nsv7063463

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,103,303

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 15542 SVs from 123 studies. See in: genome view    
    Submitted genomic75,234,241-81,337,543Question Mark
    Overlapping variant regions from other studies: 15543 SVs from 123 studies. See in: genome view    
    Remapped(Score: Perfect):75,526,582-81,629,884Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7063463Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1575,234,24181,337,543
    nsv7063463RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1575,526,58281,629,884

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18755076inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18755076Submitted genomicNC_000015.10:g.752
    34241_81337543inv
    GRCh38 (hg38)NC_000015.10Chr1575,234,24181,337,543
    nssv18755076RemappedPerfectNC_000015.9:g.7552
    6582_81629884inv
    GRCh37.p13First PassNC_000015.9Chr1575,526,58281,629,884

    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)
    nssv187550764e-061276268
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