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nsv7002625

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,065

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 99 SVs from 20 studies. See in: genome view    
    Submitted genomic44,521,193-44,527,257Question Mark
    Overlapping variant regions from other studies: 99 SVs from 20 studies. See in: genome view    
    Remapped(Score: Good):45,025,222-45,031,290Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7002625Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1944,521,19344,527,257
    nsv7002625RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1945,025,22245,031,290

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18423854deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18423854Submitted genomicNC_000019.10:g.445
    21193_44527257del
    GRCh38 (hg38)NC_000019.10Chr1944,521,19344,527,257
    nssv18423854RemappedGoodNC_000019.9:g.4502
    5222_45031290del
    GRCh37.p13First PassNC_000019.9Chr1945,025,22245,031,290

    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)
    nssv184238544e-061276046
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