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nsv6730721

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,635

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 351 SVs from 53 studies. See in: genome view    
    Submitted genomic1,378,542-1,382,176Question Mark
    Overlapping variant regions from other studies: 351 SVs from 53 studies. See in: genome view    
    Remapped(Score: Perfect):1,372,330-1,375,964Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6730721Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr41,378,5421,382,176
    nsv6730721RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr41,372,3301,375,964

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18490945deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18490945Submitted genomicNC_000004.12:g.137
    8542_1382176del
    GRCh38 (hg38)NC_000004.12Chr41,378,5421,382,176
    nssv18490945RemappedPerfectNC_000004.11:g.137
    2330_1375964del
    GRCh37.p13First PassNC_000004.11Chr41,372,3301,375,964

    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)
    nssv184909451.1e-053274706
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