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nsv6975558

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:36,100

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 393 SVs from 71 studies. See in: genome view    
    Submitted genomic85,988,701-86,024,800Question Mark
    Overlapping variant regions from other studies: 393 SVs from 71 studies. See in: genome view    
    Remapped(Score: Perfect):86,455,045-86,491,144Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6975558Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1485,988,70186,024,800
    nsv6975558RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1486,455,04586,491,144

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18391501deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18391501Submitted genomicNC_000014.9:g.8598
    8701_86024800del
    GRCh38 (hg38)NC_000014.9Chr1485,988,70186,024,800
    nssv18391501RemappedPerfectNC_000014.8:g.8645
    5045_86491144del
    GRCh37.p13First PassNC_000014.8Chr1486,455,04586,491,144

    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)
    nssv183915010.012424246726
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