U.S. flag

An official website of the United States government

nsv7063754

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,786

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 120 SVs from 28 studies. See in: genome view    
    Submitted genomic40,888,426-40,898,211Question Mark
    Overlapping variant regions from other studies: 120 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):41,180,624-41,190,409Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7063754Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1540,888,42640,898,211
    nsv7063754RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1541,180,62441,190,409

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18754756inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18754756Submitted genomicNC_000015.10:g.408
    88426_40898211inv
    GRCh38 (hg38)NC_000015.10Chr1540,888,42640,898,211
    nssv18754756RemappedPerfectNC_000015.9:g.4118
    0624_41190409inv
    GRCh37.p13First PassNC_000015.9Chr1541,180,62441,190,409

    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)
    nssv18754756<0.00163275774
    Support Center