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nsv7008977

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,235,977

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 3618 SVs from 96 studies. See in: genome view    
    Submitted genomic4,351,306-5,587,282Question Mark
    Overlapping variant regions from other studies: 3619 SVs from 96 studies. See in: genome view    
    Remapped(Score: Perfect):4,331,953-5,567,928Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7008977Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr204,351,3065,587,282
    nsv7008977RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr204,331,9535,567,928

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18431791deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18431791Submitted genomicNC_000020.11:g.435
    1306_5587282del
    GRCh38 (hg38)NC_000020.11Chr204,351,3065,587,282
    nssv18431791RemappedPerfectNC_000020.10:g.433
    1953_5567928del
    GRCh37.p13First PassNC_000020.10Chr204,331,9535,567,928

    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)
    nssv184317914e-061275804
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