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nsv6956057

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,563,645

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3928 SVs from 92 studies. See in: genome view    
    Submitted genomic86,803,289-88,366,933Question Mark
    Overlapping variant regions from other studies: 3928 SVs from 92 studies. See in: genome view    
    Remapped(Score: Perfect):87,455,544-89,019,188Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6956057Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000013.11Chr1386,803,28988,366,933
    nsv6956057RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000013.10Chr1387,455,54489,019,188

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18382350deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18382350Submitted genomicNC_000013.11:g.868
    03289_88366933del
    GRCh38 (hg38)NC_000013.11Chr1386,803,28988,366,933
    nssv18382350RemappedPerfectNC_000013.10:g.874
    55544_89019188del
    GRCh37.p13First PassNC_000013.10Chr1387,455,54489,019,188

    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)
    nssv183823501.4e-054276180
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