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nsv6711111

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,657

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 138 SVs from 22 studies. See in: genome view    
    Submitted genomic30,751,458-30,757,114Question Mark
    Overlapping variant regions from other studies: 138 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):30,792,950-30,798,606Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6711111Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr330,751,45830,757,114
    nsv6711111RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr330,792,95030,798,606

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18482525deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18482525Submitted genomicNC_000003.12:g.307
    51458_30757114del
    GRCh38 (hg38)NC_000003.12Chr330,751,45830,757,114
    nssv18482525RemappedPerfectNC_000003.11:g.307
    92950_30798606del
    GRCh37.p13First PassNC_000003.11Chr330,792,95030,798,606

    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)
    nssv184825254e-061276084
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