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nsv6376056

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:727

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 132 SVs from 22 studies. See in: genome view    
    Submitted genomic155,767,437-155,768,163Question Mark
    Overlapping variant regions from other studies: 132 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):156,688,589-156,689,315Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6376056Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4155,767,437155,768,163
    nsv6376056RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4156,688,589156,689,315

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18110262deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18110262Submitted genomicNC_000004.12:g.155
    767437_155768163de
    l
    GRCh38 (hg38)NC_000004.12Chr4155,767,437155,768,163
    nssv18110262RemappedPerfectNC_000004.11:g.156
    688589_156689315de
    l
    GRCh37.p13First PassNC_000004.11Chr4156,688,589156,689,315

    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)
    nssv18110262<0.0011737670
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