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nsv7012452

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,956,182

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 11189 SVs from 108 studies. See in: genome view    
    Submitted genomic45,998,776-48,954,957Question Mark
    Overlapping variant regions from other studies: 11190 SVs from 108 studies. See in: genome view    
    Remapped(Score: Perfect):46,502,034-49,458,214Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv7012452Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1945,998,77648,954,957
    nsv7012452RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1946,502,03449,458,214

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18425268deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18425268Submitted genomicNC_000019.10:g.459
    98776_48954957del
    GRCh38 (hg38)NC_000019.10Chr1945,998,77648,954,957
    nssv18425268RemappedPerfectNC_000019.9:g.4650
    2034_49458214del
    GRCh37.p13First PassNC_000019.9Chr1946,502,03449,458,214

    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)
    nssv184252682.8e-058275272
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