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nsv6903946

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,480

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 84 SVs from 26 studies. See in: genome view    
    Submitted genomic68,075,487-68,079,966Question Mark
    Overlapping variant regions from other studies: 84 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):67,842,954-67,847,433Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6903946Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1168,075,48768,079,966
    nsv6903946RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1167,842,95467,847,433

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18351385deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18351385Submitted genomicNC_000011.10:g.680
    75487_68079966del
    GRCh38 (hg38)NC_000011.10Chr1168,075,48768,079,966
    nssv18351385RemappedPerfectNC_000011.9:g.6784
    2954_67847433del
    GRCh37.p13First PassNC_000011.9Chr1167,842,95467,847,433

    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)
    nssv183513854e-061276070
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