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nsv6529768

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,901

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 126 SVs from 36 studies. See in: genome view    
    Submitted genomic50,048,023-50,049,923Question Mark
    Overlapping variant regions from other studies: 126 SVs from 36 studies. See in: genome view    
    Remapped(Score: Perfect):50,551,280-50,553,180Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6529768Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1950,048,02350,049,923
    nsv6529768RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1950,551,28050,553,180

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18049072deletionSequencingSequence alignment

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18049072Submitted genomicNC_000019.10:g.500
    48023_50049923del
    GRCh38 (hg38)NC_000019.10Chr1950,048,02350,049,923
    nssv18049072RemappedPerfectNC_000019.9:g.5055
    1280_50553180del
    GRCh37.p13First PassNC_000019.9Chr1950,551,28050,553,180

    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)
    nssv18049072<0.001238858
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