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nsv7073892

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:47,391

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 392 SVs from 53 studies. See in: genome view    
    Submitted genomic56,132,437-56,179,827Question Mark
    Overlapping variant regions from other studies: 392 SVs from 53 studies. See in: genome view    
    Remapped(Score: Perfect):56,643,806-56,691,196Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7073892Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1956,132,43756,179,827
    nsv7073892RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1956,643,80656,691,196

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18761359inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18761359Submitted genomicNC_000019.10:g.561
    32437_56179827inv
    GRCh38 (hg38)NC_000019.10Chr1956,132,43756,179,827
    nssv18761359RemappedPerfectNC_000019.9:g.5664
    3806_56691196inv
    GRCh37.p13First PassNC_000019.9Chr1956,643,80656,691,196

    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)
    nssv187613594e-061276268
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