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nsv6720678

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:43,800

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 155 SVs from 41 studies. See in: genome view    
    Submitted genomic44,022,001-44,065,800Question Mark
    Overlapping variant regions from other studies: 155 SVs from 41 studies. See in: genome view    
    Remapped(Score: Perfect):44,024,018-44,067,817Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6720678Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr444,022,00144,065,800
    nsv6720678RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr444,024,01844,067,817

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18495398deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18495398Submitted genomicNC_000004.12:g.440
    22001_44065800del
    GRCh38 (hg38)NC_000004.12Chr444,022,00144,065,800
    nssv18495398RemappedPerfectNC_000004.11:g.440
    24018_44067817del
    GRCh37.p13First PassNC_000004.11Chr444,024,01844,067,817

    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)
    nssv18495398<0.00198245632
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