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nsv6937405

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:329,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 778 SVs from 73 studies. See in: genome view    
    Submitted genomic87,957,217-88,286,316Question Mark
    Overlapping variant regions from other studies: 778 SVs from 73 studies. See in: genome view    
    Remapped(Score: Perfect):88,350,994-88,680,093Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6937405Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1287,957,21788,286,316
    nsv6937405RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1288,350,99488,680,093

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18373566deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18373566Submitted genomicNC_000012.12:g.879
    57217_88286316del
    GRCh38 (hg38)NC_000012.12Chr1287,957,21788,286,316
    nssv18373566RemappedPerfectNC_000012.11:g.883
    50994_88680093del
    GRCh37.p13First PassNC_000012.11Chr1288,350,99488,680,093

    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)
    nssv183735664e-061274894
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