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nsv7003434

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,181

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 143 SVs from 34 studies. See in: genome view    
    Submitted genomic4,371,674-4,378,854Question Mark
    Overlapping variant regions from other studies: 143 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):4,371,671-4,378,851Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7003434Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr194,371,6744,378,854
    nsv7003434RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr194,371,6714,378,851

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18423998deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18423998Submitted genomicNC_000019.10:g.437
    1674_4378854del
    GRCh38 (hg38)NC_000019.10Chr194,371,6744,378,854
    nssv18423998RemappedPerfectNC_000019.9:g.4371
    671_4378851del
    GRCh37.p13First PassNC_000019.9Chr194,371,6714,378,851

    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)
    nssv184239987e-062276230
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