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nsv6775061

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:74

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 80 SVs from 16 studies. See in: genome view    
    Submitted genomic75,922,938-75,923,011Question Mark
    Overlapping variant regions from other studies: 80 SVs from 16 studies. See in: genome view    
    Remapped(Score: Perfect):75,218,763-75,218,836Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6775061Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr575,922,93875,923,011
    nsv6775061RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr575,218,76375,218,836

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18516367deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18516367Submitted genomicNC_000005.10:g.759
    22938_75923011del
    GRCh38 (hg38)NC_000005.10Chr575,922,93875,923,011
    nssv18516367RemappedPerfectNC_000005.9:g.7521
    8763_75218836del
    GRCh37.p13First PassNC_000005.9Chr575,218,76375,218,836

    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)
    nssv18516367<0.001117259670
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