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nsv7044056

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:272,228

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 1313 SVs from 93 studies. See in: genome view    
    Submitted genomic97,612,443-97,884,670Question Mark
    Overlapping variant regions from other studies: 1313 SVs from 93 studies. See in: genome view    
    Remapped(Score: Perfect):96,948,147-97,220,374Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7044056Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr597,612,44397,884,670
    nsv7044056RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr596,948,14797,220,374

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18777063inversionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18777063Submitted genomicNC_000005.10:g.976
    12443_97884670inv
    GRCh38 (hg38)NC_000005.10Chr597,612,44397,884,670
    nssv18777063RemappedPerfectNC_000005.9:g.9694
    8147_97220374inv
    GRCh37.p13First PassNC_000005.9Chr596,948,14797,220,374

    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)
    nssv187770634e-061276268
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