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nsv7058481

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:20,549

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 137 SVs from 29 studies. See in: genome view    
    Submitted genomic88,216,038-88,236,586Question Mark
    Overlapping variant regions from other studies: 137 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):88,759,269-88,779,817Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7058481Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1588,216,03888,236,586
    nsv7058481RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1588,759,26988,779,817

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18756087inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18756087Submitted genomicNC_000015.10:g.882
    16038_88236586inv
    GRCh38 (hg38)NC_000015.10Chr1588,216,03888,236,586
    nssv18756087RemappedPerfectNC_000015.9:g.8875
    9269_88779817inv
    GRCh37.p13First PassNC_000015.9Chr1588,759,26988,779,817

    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)
    nssv187560874e-061276268
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