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nsv7008827

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 151 SVs from 38 studies. See in: genome view    
    Submitted genomic4,328,418-4,328,482Question Mark
    Overlapping variant regions from other studies: 151 SVs from 38 studies. See in: genome view    
    Remapped(Score: Perfect):4,328,415-4,328,479Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7008827Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr194,328,4184,328,482
    nsv7008827RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr194,328,4154,328,479

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18423954deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18423954Submitted genomicNC_000019.10:g.432
    8418_4328482del
    GRCh38 (hg38)NC_000019.10Chr194,328,4184,328,482
    nssv18423954RemappedPerfectNC_000019.9:g.4328
    415_4328479del
    GRCh37.p13First PassNC_000019.9Chr194,328,4154,328,479

    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)
    nssv184239540.30261151203022
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