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nsv6654959

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:275

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 164 SVs from 44 studies. See in: genome view    
    Submitted genomic76,634,690-76,634,964Question Mark
    Overlapping variant regions from other studies: 164 SVs from 44 studies. See in: genome view    
    Remapped(Score: Perfect):77,100,375-77,100,649Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6654959Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr176,634,69076,634,964
    nsv6654959RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr177,100,37577,100,649

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18427247deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18427247Submitted genomicNC_000001.11:g.766
    34690_76634964del
    GRCh38 (hg38)NC_000001.11Chr176,634,69076,634,964
    nssv18427247RemappedPerfectNC_000001.10:g.771
    00375_77100649del
    GRCh37.p13First PassNC_000001.10Chr177,100,37577,100,649

    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)
    nssv184272470.607135720224722
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