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nsv7021430

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,090

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 146 SVs from 23 studies. See in: genome view    
    Submitted genomic44,373,862-44,379,951Question Mark
    Overlapping variant regions from other studies: 146 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):43,002,502-43,008,591Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7021430Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2044,373,86244,379,951
    nsv7021430RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2043,002,50243,008,591

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18432667deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18432667Submitted genomicNC_000020.11:g.443
    73862_44379951del
    GRCh38 (hg38)NC_000020.11Chr2044,373,86244,379,951
    nssv18432667RemappedPerfectNC_000020.10:g.430
    02502_43008591del
    GRCh37.p13First PassNC_000020.10Chr2043,002,50243,008,591

    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)
    nssv184326672.8e-058276136
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