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nsv6930898

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,970

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 113 SVs from 22 studies. See in: genome view    
    Submitted genomic9,074,786-9,076,755Question Mark
    Overlapping variant regions from other studies: 113 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):9,227,382-9,229,351Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6930898Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr129,074,7869,076,755
    nsv6930898RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr129,227,3829,229,351

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18373993deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18373993Submitted genomicNC_000012.12:g.907
    4786_9076755del
    GRCh38 (hg38)NC_000012.12Chr129,074,7869,076,755
    nssv18373993RemappedPerfectNC_000012.11:g.922
    7382_9229351del
    GRCh37.p13First PassNC_000012.11Chr129,227,3829,229,351

    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)
    nssv183739937e-062275480
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